/bookmark_gr.pngookmark_gr.pngkmark_gr.pnggr.png.pngngitle class="wrap-content-read table-responsive">lass="wrap-content-read table-responsive">ss="wrap-content-read table-responsive">="wrap-content-read table-responsive">wrap-content-read table-responsive">ap-content-read table-responsive">-content-read table-responsive">tent-read table-responsive">nt-read table-responsive">-read table-responsive">d table-responsive">table-responsive">responsive">sponsive">onsive"> classass9785970407042-0028-00085970407042-0028-000970407042-0028-0000407042-0028-00007042-0028-000042-0028-000028-0008-000000b>span>prise a class of structurally related proteins of immunoglobulin superfamily with two types of paired polypeptide chains namely: light (L) of low molecular mass, and heavy (H) of high molecular mass. All 4 chains are bound by disulfide bonds. There are two types of the light chain constant regions designated as к and X. There are five main forms of the heavy chain constant regions designated as follows: u, y, 8, а, and e. Each form is associated with separate Ig class. Based on structural and antigenic features of their H-chains Ig are divided (listed in order of their percentage in blood) into 5 classes: IgG (up to 85%), IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.ise a class of structurally related proteins of immunoglobulin superfamily with two types of paired polypeptide chains namely: light (L) of low molecular mass, and heavy (H) of high molecular mass. All 4 chains are bound by disulfide bonds. There are two types of the light chain constant regions designated as к and X. There are five main forms of the heavy chain constant regions designated as follows: u, y, 8, а, and e. Each form is associated with separate Ig class. Based on structural and antigenic features of their H-chains Ig are divided (listed in order of their percentage in blood) into 5 classes: IgG (up to 85%), IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.e a class of structurally related proteins of immunoglobulin superfamily with two types of paired polypeptide chains namely: light (L) of low molecular mass, and heavy (H) of high molecular mass. All 4 chains are bound by disulfide bonds. There are two types of the light chain constant regions designated as к and X. There are five main forms of the heavy chain constant regions designated as follows: u, y, 8, а, and e. Each form is associated with separate Ig class. Based on structural and antigenic features of their H-chains Ig are divided (listed in order of their percentage in blood) into 5 classes: IgG (up to 85%), IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.a class of structurally related proteins of immunoglobulin superfamily with two types of paired polypeptide chains namely: light (L) of low molecular mass, and heavy (H) of high molecular mass. All 4 chains are bound by disulfide bonds. There are two types of the light chain constant regions designated as к and X. There are five main forms of the heavy chain constant regions designated as follows: u, y, 8, а, and e. Each form is associated with separate Ig class. Based on structural and antigenic features of their H-chains Ig are divided (listed in order of their percentage in blood) into 5 classes: IgG (up to 85%), IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.class of structurally related proteins of immunoglobulin superfamily with two types of paired polypeptide chains namely: light (L) of low molecular mass, and heavy (H) of high molecular mass. All 4 chains are bound by disulfide bonds. There are two types of the light chain constant regions designated as к and X. There are five main forms of the heavy chain constant regions designated as follows: u, y, 8, а, and e. Each form is associated with separate Ig class. Based on structural and antigenic features of their H-chains Ig are divided (listed in order of their percentage in blood) into 5 classes: IgG (up to 85%), IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.ass of structurally related proteins of immunoglobulin superfamily with two types of paired polypeptide chains namely: light (L) of low molecular mass, and heavy (H) of high molecular mass. All 4 chains are bound by disulfide bonds. There are two types of the light chain constant regions designated as к and X. There are five main forms of the heavy chain constant regions designated as follows: u, y, 8, а, and e. Each form is associated with separate Ig class. Based on structural and antigenic features of their H-chains Ig are divided (listed in order of their percentage in blood) into 5 classes: IgG (up to 85%), IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.of structurally related proteins of immunoglobulin superfamily with two types of paired polypeptide chains namely: light (L) of low molecular mass, and heavy (H) of high molecular mass. All 4 chains are bound by disulfide bonds. There are two types of the light chain constant regions designated as к and X. There are five main forms of the heavy chain constant regions designated as follows: u, y, 8, а, and e. Each form is associated with separate Ig class. Based on structural and antigenic features of their H-chains Ig are divided (listed in order of their percentage in blood) into 5 classes: IgG (up to 85%), IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person. structurally related proteins of immunoglobulin superfamily with two types of paired polypeptide chains namely: light (L) of low molecular mass, and heavy (H) of high molecular mass. All 4 chains are bound by disulfide bonds. There are two types of the light chain constant regions designated as к and X. There are five main forms of the heavy chain constant regions designated as follows: u, y, 8, а, and e. Each form is associated with separate Ig class. Based on structural and antigenic features of their H-chains Ig are divided (listed in order of their percentage in blood) into 5 classes: IgG (up to 85%), IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.tructurally related proteins of immunoglobulin superfamily with two types of paired polypeptide chains namely: light (L) of low molecular mass, and heavy (H) of high molecular mass. All 4 chains are bound by disulfide bonds. There are two types of the light chain constant regions designated as к and X. There are five main forms of the heavy chain constant regions designated as follows: u, y, 8, а, and e. Each form is associated with separate Ig class. Based on structural and antigenic features of their H-chains Ig are divided (listed in order of their percentage in blood) into 5 classes: IgG (up to 85%), IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.turally related proteins of immunoglobulin superfamily with two types of paired polypeptide chains namely: light (L) of low molecular mass, and heavy (H) of high molecular mass. All 4 chains are bound by disulfide bonds. There are two types of the light chain constant regions designated as к and X. There are five main forms of the heavy chain constant regions designated as follows: u, y, 8, а, and e. Each form is associated with separate Ig class. Based on structural and antigenic features of their H-chains Ig are divided (listed in order of their percentage in blood) into 5 classes: IgG (up to 85%), IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.rally related proteins of immunoglobulin superfamily with two types of paired polypeptide chains namely: light (L) of low molecular mass, and heavy (H) of high molecular mass. All 4 chains are bound by disulfide bonds. There are two types of the light chain constant regions designated as к and X. There are five main forms of the heavy chain constant regions designated as follows: u, y, 8, а, and e. Each form is associated with separate Ig class. Based on structural and antigenic features of their H-chains Ig are divided (listed in order of their percentage in blood) into 5 classes: IgG (up to 85%), IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.related proteins of immunoglobulin superfamily with two types of paired polypeptide chains namely: light (L) of low molecular mass, and heavy (H) of high molecular mass. All 4 chains are bound by disulfide bonds. There are two types of the light chain constant regions designated as к and X. There are five main forms of the heavy chain constant regions designated as follows: u, y, 8, а, and e. Each form is associated with separate Ig class. Based on structural and antigenic features of their H-chains Ig are divided (listed in order of their percentage in blood) into 5 classes: IgG (up to 85%), IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.lated proteins of immunoglobulin superfamily with two types of paired polypeptide chains namely: light (L) of low molecular mass, and heavy (H) of high molecular mass. All 4 chains are bound by disulfide bonds. There are two types of the light chain constant regions designated as к and X. There are five main forms of the heavy chain constant regions designated as follows: u, y, 8, а, and e. Each form is associated with separate Ig class. Based on structural and antigenic features of their H-chains Ig are divided (listed in order of their percentage in blood) into 5 classes: IgG (up to 85%), IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.ted proteins of immunoglobulin superfamily with two types of paired polypeptide chains namely: light (L) of low molecular mass, and heavy (H) of high molecular mass. All 4 chains are bound by disulfide bonds. There are two types of the light chain constant regions designated as к and X. There are five main forms of the heavy chain constant regions designated as follows: u, y, 8, а, and e. Each form is associated with separate Ig class. Based on structural and antigenic features of their H-chains Ig are divided (listed in order of their percentage in blood) into 5 classes: IgG (up to 85%), IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person. immunoglobulin superfamily with two types of paired polypeptide chains namely: light (L) of low molecular mass, and heavy (H) of high molecular mass. All 4 chains are bound by disulfide bonds. There are two types of the light chain constant regions designated as к and X. There are five main forms of the heavy chain constant regions designated as follows: u, y, 8, а, and e. Each form is associated with separate Ig class. Based on structural and antigenic features of their H-chains Ig are divided (listed in order of their percentage in blood) into 5 classes: IgG (up to 85%), IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.mmunoglobulin superfamily with two types of paired polypeptide chains namely: light (L) of low molecular mass, and heavy (H) of high molecular mass. All 4 chains are bound by disulfide bonds. There are two types of the light chain constant regions designated as к and X. There are five main forms of the heavy chain constant regions designated as follows: u, y, 8, а, and e. Each form is associated with separate Ig class. Based on structural and antigenic features of their H-chains Ig are divided (listed in order of their percentage in blood) into 5 classes: IgG (up to 85%), IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.unoglobulin superfamily with two types of paired polypeptide chains namely: light (L) of low molecular mass, and heavy (H) of high molecular mass. All 4 chains are bound by disulfide bonds. There are two types of the light chain constant regions designated as к and X. There are five main forms of the heavy chain constant regions designated as follows: u, y, 8, а, and e. Each form is associated with separate Ig class. Based on structural and antigenic features of their H-chains Ig are divided (listed in order of their percentage in blood) into 5 classes: IgG (up to 85%), IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.globulin superfamily with two types of paired polypeptide chains namely: light (L) of low molecular mass, and heavy (H) of high molecular mass. All 4 chains are bound by disulfide bonds. There are two types of the light chain constant regions designated as к and X. There are five main forms of the heavy chain constant regions designated as follows: u, y, 8, а, and e. Each form is associated with separate Ig class. Based on structural and antigenic features of their H-chains Ig are divided (listed in order of their percentage in blood) into 5 classes: IgG (up to 85%), IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.obulin superfamily with two types of paired polypeptide chains namely: light (L) of low molecular mass, and heavy (H) of high molecular mass. All 4 chains are bound by disulfide bonds. There are two types of the light chain constant regions designated as к and X. There are five main forms of the heavy chain constant regions designated as follows: u, y, 8, а, and e. Each form is associated with separate Ig class. Based on structural and antigenic features of their H-chains Ig are divided (listed in order of their percentage in blood) into 5 classes: IgG (up to 85%), IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.ulin superfamily with two types of paired polypeptide chains namely: light (L) of low molecular mass, and heavy (H) of high molecular mass. All 4 chains are bound by disulfide bonds. There are two types of the light chain constant regions designated as к and X. There are five main forms of the heavy chain constant regions designated as follows: u, y, 8, а, and e. Each form is associated with separate Ig class. Based on structural and antigenic features of their H-chains Ig are divided (listed in order of their percentage in blood) into 5 classes: IgG (up to 85%), IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.s of paired polypeptide chains namely: light (L) of low molecular mass, and heavy (H) of high molecular mass. All 4 chains are bound by disulfide bonds. There are two types of the light chain constant regions designated as к and X. There are five main forms of the heavy chain constant regions designated as follows: u, y, 8, а, and e. Each form is associated with separate Ig class. Based on structural and antigenic features of their H-chains Ig are divided (listed in order of their percentage in blood) into 5 classes: IgG (up to 85%), IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.of paired polypeptide chains namely: light (L) of low molecular mass, and heavy (H) of high molecular mass. All 4 chains are bound by disulfide bonds. There are two types of the light chain constant regions designated as к and X. There are five main forms of the heavy chain constant regions designated as follows: u, y, 8, а, and e. Each form is associated with separate Ig class. Based on structural and antigenic features of their H-chains Ig are divided (listed in order of their percentage in blood) into 5 classes: IgG (up to 85%), IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person. paired polypeptide chains namely: light (L) of low molecular mass, and heavy (H) of high molecular mass. All 4 chains are bound by disulfide bonds. There are two types of the light chain constant regions designated as к and X. There are five main forms of the heavy chain constant regions designated as follows: u, y, 8, а, and e. Each form is associated with separate Ig class. Based on structural and antigenic features of their H-chains Ig are divided (listed in order of their percentage in blood) into 5 classes: IgG (up to 85%), IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.aired polypeptide chains namely: light (L) of low molecular mass, and heavy (H) of high molecular mass. All 4 chains are bound by disulfide bonds. There are two types of the light chain constant regions designated as к and X. There are five main forms of the heavy chain constant regions designated as follows: u, y, 8, а, and e. Each form is associated with separate Ig class. Based on structural and antigenic features of their H-chains Ig are divided (listed in order of their percentage in blood) into 5 classes: IgG (up to 85%), IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.red polypeptide chains namely: light (L) of low molecular mass, and heavy (H) of high molecular mass. All 4 chains are bound by disulfide bonds. There are two types of the light chain constant regions designated as к and X. There are five main forms of the heavy chain constant regions designated as follows: u, y, 8, а, and e. Each form is associated with separate Ig class. Based on structural and antigenic features of their H-chains Ig are divided (listed in order of their percentage in blood) into 5 classes: IgG (up to 85%), IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.d polypeptide chains namely: light (L) of low molecular mass, and heavy (H) of high molecular mass. All 4 chains are bound by disulfide bonds. There are two types of the light chain constant regions designated as к and X. There are five main forms of the heavy chain constant regions designated as follows: u, y, 8, а, and e. Each form is associated with separate Ig class. Based on structural and antigenic features of their H-chains Ig are divided (listed in order of their percentage in blood) into 5 classes: IgG (up to 85%), IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.ypeptide chains namely: light (L) of low molecular mass, and heavy (H) of high molecular mass. All 4 chains are bound by disulfide bonds. There are two types of the light chain constant regions designated as к and X. There are five main forms of the heavy chain constant regions designated as follows: u, y, 8, а, and e. Each form is associated with separate Ig class. Based on structural and antigenic features of their H-chains Ig are divided (listed in order of their percentage in blood) into 5 classes: IgG (up to 85%), IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.eptide chains namely: light (L) of low molecular mass, and heavy (H) of high molecular mass. All 4 chains are bound by disulfide bonds. There are two types of the light chain constant regions designated as к and X. There are five main forms of the heavy chain constant regions designated as follows: u, y, 8, а, and e. Each form is associated with separate Ig class. Based on structural and antigenic features of their H-chains Ig are divided (listed in order of their percentage in blood) into 5 classes: IgG (up to 85%), IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.tide chains namely: light (L) of low molecular mass, and heavy (H) of high molecular mass. All 4 chains are bound by disulfide bonds. There are two types of the light chain constant regions designated as к and X. There are five main forms of the heavy chain constant regions designated as follows: u, y, 8, а, and e. Each form is associated with separate Ig class. Based on structural and antigenic features of their H-chains Ig are divided (listed in order of their percentage in blood) into 5 classes: IgG (up to 85%), IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.of high molecular mass. All 4 chains are bound by disulfide bonds. There are two types of the light chain constant regions designated as к and X. There are five main forms of the heavy chain constant regions designated as follows: u, y, 8, а, and e. Each form is associated with separate Ig class. Based on structural and antigenic features of their H-chains Ig are divided (listed in order of their percentage in blood) into 5 classes: IgG (up to 85%), IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person. high molecular mass. All 4 chains are bound by disulfide bonds. There are two types of the light chain constant regions designated as к and X. There are five main forms of the heavy chain constant regions designated as follows: u, y, 8, а, and e. Each form is associated with separate Ig class. Based on structural and antigenic features of their H-chains Ig are divided (listed in order of their percentage in blood) into 5 classes: IgG (up to 85%), IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.igh molecular mass. All 4 chains are bound by disulfide bonds. There are two types of the light chain constant regions designated as к and X. There are five main forms of the heavy chain constant regions designated as follows: u, y, 8, а, and e. Each form is associated with separate Ig class. Based on structural and antigenic features of their H-chains Ig are divided (listed in order of their percentage in blood) into 5 classes: IgG (up to 85%), IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.lecular mass. All 4 chains are bound by disulfide bonds. There are two types of the light chain constant regions designated as к and X. There are five main forms of the heavy chain constant regions designated as follows: u, y, 8, а, and e. Each form is associated with separate Ig class. Based on structural and antigenic features of their H-chains Ig are divided (listed in order of their percentage in blood) into 5 classes: IgG (up to 85%), IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.cular mass. All 4 chains are bound by disulfide bonds. There are two types of the light chain constant regions designated as к and X. There are five main forms of the heavy chain constant regions designated as follows: u, y, 8, а, and e. Each form is associated with separate Ig class. Based on structural and antigenic features of their H-chains Ig are divided (listed in order of their percentage in blood) into 5 classes: IgG (up to 85%), IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.lar mass. All 4 chains are bound by disulfide bonds. There are two types of the light chain constant regions designated as к and X. There are five main forms of the heavy chain constant regions designated as follows: u, y, 8, а, and e. Each form is associated with separate Ig class. Based on structural and antigenic features of their H-chains Ig are divided (listed in order of their percentage in blood) into 5 classes: IgG (up to 85%), IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.hains are bound by disulfide bonds. There are two types of the light chain constant regions designated as к and X. There are five main forms of the heavy chain constant regions designated as follows: u, y, 8, а, and e. Each form is associated with separate Ig class. Based on structural and antigenic features of their H-chains Ig are divided (listed in order of their percentage in blood) into 5 classes: IgG (up to 85%), IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.ins are bound by disulfide bonds. There are two types of the light chain constant regions designated as к and X. There are five main forms of the heavy chain constant regions designated as follows: u, y, 8, а, and e. Each form is associated with separate Ig class. Based on structural and antigenic features of their H-chains Ig are divided (listed in order of their percentage in blood) into 5 classes: IgG (up to 85%), IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.s are bound by disulfide bonds. There are two types of the light chain constant regions designated as к and X. There are five main forms of the heavy chain constant regions designated as follows: u, y, 8, а, and e. Each form is associated with separate Ig class. Based on structural and antigenic features of their H-chains Ig are divided (listed in order of their percentage in blood) into 5 classes: IgG (up to 85%), IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.of the light chain constant regions designated as к and X. There are five main forms of the heavy chain constant regions designated as follows: u, y, 8, а, and e. Each form is associated with separate Ig class. Based on structural and antigenic features of their H-chains Ig are divided (listed in order of their percentage in blood) into 5 classes: IgG (up to 85%), IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person. the light chain constant regions designated as к and X. There are five main forms of the heavy chain constant regions designated as follows: u, y, 8, а, and e. Each form is associated with separate Ig class. Based on structural and antigenic features of their H-chains Ig are divided (listed in order of their percentage in blood) into 5 classes: IgG (up to 85%), IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.he light chain constant regions designated as к and X. There are five main forms of the heavy chain constant regions designated as follows: u, y, 8, а, and e. Each form is associated with separate Ig class. Based on structural and antigenic features of their H-chains Ig are divided (listed in order of their percentage in blood) into 5 classes: IgG (up to 85%), IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person. light chain constant regions designated as к and X. There are five main forms of the heavy chain constant regions designated as follows: u, y, 8, а, and e. Each form is associated with separate Ig class. Based on structural and antigenic features of their H-chains Ig are divided (listed in order of their percentage in blood) into 5 classes: IgG (up to 85%), IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.ight chain constant regions designated as к and X. There are five main forms of the heavy chain constant regions designated as follows: u, y, 8, а, and e. Each form is associated with separate Ig class. Based on structural and antigenic features of their H-chains Ig are divided (listed in order of their percentage in blood) into 5 classes: IgG (up to 85%), IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.ht chain constant regions designated as к and X. There are five main forms of the heavy chain constant regions designated as follows: u, y, 8, а, and e. Each form is associated with separate Ig class. Based on structural and antigenic features of their H-chains Ig are divided (listed in order of their percentage in blood) into 5 classes: IgG (up to 85%), IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person. chain constant regions designated as к and X. There are five main forms of the heavy chain constant regions designated as follows: u, y, 8, а, and e. Each form is associated with separate Ig class. Based on structural and antigenic features of their H-chains Ig are divided (listed in order of their percentage in blood) into 5 classes: IgG (up to 85%), IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.in constant regions designated as к and X. There are five main forms of the heavy chain constant regions designated as follows: u, y, 8, а, and e. Each form is associated with separate Ig class. Based on structural and antigenic features of their H-chains Ig are divided (listed in order of their percentage in blood) into 5 classes: IgG (up to 85%), IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person. constant regions designated as к and X. There are five main forms of the heavy chain constant regions designated as follows: u, y, 8, а, and e. Each form is associated with separate Ig class. Based on structural and antigenic features of their H-chains Ig are divided (listed in order of their percentage in blood) into 5 classes: IgG (up to 85%), IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.onstant regions designated as к and X. There are five main forms of the heavy chain constant regions designated as follows: u, y, 8, а, and e. Each form is associated with separate Ig class. Based on structural and antigenic features of their H-chains Ig are divided (listed in order of their percentage in blood) into 5 classes: IgG (up to 85%), IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.ant regions designated as к and X. There are five main forms of the heavy chain constant regions designated as follows: u, y, 8, а, and e. Each form is associated with separate Ig class. Based on structural and antigenic features of their H-chains Ig are divided (listed in order of their percentage in blood) into 5 classes: IgG (up to 85%), IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.t regions designated as к and X. There are five main forms of the heavy chain constant regions designated as follows: u, y, 8, а, and e. Each form is associated with separate Ig class. Based on structural and antigenic features of their H-chains Ig are divided (listed in order of their percentage in blood) into 5 classes: IgG (up to 85%), IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.ons designated as к and X. There are five main forms of the heavy chain constant regions designated as follows: u, y, 8, а, and e. Each form is associated with separate Ig class. Based on structural and antigenic features of their H-chains Ig are divided (listed in order of their percentage in blood) into 5 classes: IgG (up to 85%), IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.s designated as к and X. There are five main forms of the heavy chain constant regions designated as follows: u, y, 8, а, and e. Each form is associated with separate Ig class. Based on structural and antigenic features of their H-chains Ig are divided (listed in order of their percentage in blood) into 5 classes: IgG (up to 85%), IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.designated as к and X. There are five main forms of the heavy chain constant regions designated as follows: u, y, 8, а, and e. Each form is associated with separate Ig class. Based on structural and antigenic features of their H-chains Ig are divided (listed in order of their percentage in blood) into 5 classes: IgG (up to 85%), IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.� and X. There are five main forms of the heavy chain constant regions designated as follows: u, y, 8, а, and e. Each form is associated with separate Ig class. Based on structural and antigenic features of their H-chains Ig are divided (listed in order of their percentage in blood) into 5 classes: IgG (up to 85%), IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.and X. There are five main forms of the heavy chain constant regions designated as follows: u, y, 8, а, and e. Each form is associated with separate Ig class. Based on structural and antigenic features of their H-chains Ig are divided (listed in order of their percentage in blood) into 5 classes: IgG (up to 85%), IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.d X. There are five main forms of the heavy chain constant regions designated as follows: u, y, 8, а, and e. Each form is associated with separate Ig class. Based on structural and antigenic features of their H-chains Ig are divided (listed in order of their percentage in blood) into 5 classes: IgG (up to 85%), IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.. There are five main forms of the heavy chain constant regions designated as follows: u, y, 8, а, and e. Each form is associated with separate Ig class. Based on structural and antigenic features of their H-chains Ig are divided (listed in order of their percentage in blood) into 5 classes: IgG (up to 85%), IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.There are five main forms of the heavy chain constant regions designated as follows: u, y, 8, а, and e. Each form is associated with separate Ig class. Based on structural and antigenic features of their H-chains Ig are divided (listed in order of their percentage in blood) into 5 classes: IgG (up to 85%), IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.ere are five main forms of the heavy chain constant regions designated as follows: u, y, 8, а, and e. Each form is associated with separate Ig class. Based on structural and antigenic features of their H-chains Ig are divided (listed in order of their percentage in blood) into 5 classes: IgG (up to 85%), IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person. heavy chain constant regions designated as follows: u, y, 8, а, and e. Each form is associated with separate Ig class. Based on structural and antigenic features of their H-chains Ig are divided (listed in order of their percentage in blood) into 5 classes: IgG (up to 85%), IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.eavy chain constant regions designated as follows: u, y, 8, а, and e. Each form is associated with separate Ig class. Based on structural and antigenic features of their H-chains Ig are divided (listed in order of their percentage in blood) into 5 classes: IgG (up to 85%), IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.vy chain constant regions designated as follows: u, y, 8, а, and e. Each form is associated with separate Ig class. Based on structural and antigenic features of their H-chains Ig are divided (listed in order of their percentage in blood) into 5 classes: IgG (up to 85%), IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person. chain constant regions designated as follows: u, y, 8, а, and e. Each form is associated with separate Ig class. Based on structural and antigenic features of their H-chains Ig are divided (listed in order of their percentage in blood) into 5 classes: IgG (up to 85%), IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.hain constant regions designated as follows: u, y, 8, а, and e. Each form is associated with separate Ig class. Based on structural and antigenic features of their H-chains Ig are divided (listed in order of their percentage in blood) into 5 classes: IgG (up to 85%), IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.in constant regions designated as follows: u, y, 8, а, and e. Each form is associated with separate Ig class. Based on structural and antigenic features of their H-chains Ig are divided (listed in order of their percentage in blood) into 5 classes: IgG (up to 85%), IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.nstant regions designated as follows: u, y, 8, а, and e. Each form is associated with separate Ig class. Based on structural and antigenic features of their H-chains Ig are divided (listed in order of their percentage in blood) into 5 classes: IgG (up to 85%), IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.tant regions designated as follows: u, y, 8, а, and e. Each form is associated with separate Ig class. Based on structural and antigenic features of their H-chains Ig are divided (listed in order of their percentage in blood) into 5 classes: IgG (up to 85%), IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.nt regions designated as follows: u, y, 8, а, and e. Each form is associated with separate Ig class. Based on structural and antigenic features of their H-chains Ig are divided (listed in order of their percentage in blood) into 5 classes: IgG (up to 85%), IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.associated with separate Ig class. Based on structural and antigenic features of their H-chains Ig are divided (listed in order of their percentage in blood) into 5 classes: IgG (up to 85%), IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.sociated with separate Ig class. Based on structural and antigenic features of their H-chains Ig are divided (listed in order of their percentage in blood) into 5 classes: IgG (up to 85%), IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.ciated with separate Ig class. Based on structural and antigenic features of their H-chains Ig are divided (listed in order of their percentage in blood) into 5 classes: IgG (up to 85%), IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person. with separate Ig class. Based on structural and antigenic features of their H-chains Ig are divided (listed in order of their percentage in blood) into 5 classes: IgG (up to 85%), IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.ith separate Ig class. Based on structural and antigenic features of their H-chains Ig are divided (listed in order of their percentage in blood) into 5 classes: IgG (up to 85%), IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.h separate Ig class. Based on structural and antigenic features of their H-chains Ig are divided (listed in order of their percentage in blood) into 5 classes: IgG (up to 85%), IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.ss. Based on structural and antigenic features of their H-chains Ig are divided (listed in order of their percentage in blood) into 5 classes: IgG (up to 85%), IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.. Based on structural and antigenic features of their H-chains Ig are divided (listed in order of their percentage in blood) into 5 classes: IgG (up to 85%), IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.Based on structural and antigenic features of their H-chains Ig are divided (listed in order of their percentage in blood) into 5 classes: IgG (up to 85%), IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person. their H-chains Ig are divided (listed in order of their percentage in blood) into 5 classes: IgG (up to 85%), IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.heir H-chains Ig are divided (listed in order of their percentage in blood) into 5 classes: IgG (up to 85%), IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.ir H-chains Ig are divided (listed in order of their percentage in blood) into 5 classes: IgG (up to 85%), IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person. H-chains Ig are divided (listed in order of their percentage in blood) into 5 classes: IgG (up to 85%), IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.-chains Ig are divided (listed in order of their percentage in blood) into 5 classes: IgG (up to 85%), IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.hains Ig are divided (listed in order of their percentage in blood) into 5 classes: IgG (up to 85%), IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.ins Ig are divided (listed in order of their percentage in blood) into 5 classes: IgG (up to 85%), IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.Ig are divided (listed in order of their percentage in blood) into 5 classes: IgG (up to 85%), IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person. are divided (listed in order of their percentage in blood) into 5 classes: IgG (up to 85%), IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.re divided (listed in order of their percentage in blood) into 5 classes: IgG (up to 85%), IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.ivided (listed in order of their percentage in blood) into 5 classes: IgG (up to 85%), IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.ided (listed in order of their percentage in blood) into 5 classes: IgG (up to 85%), IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.listed in order of their percentage in blood) into 5 classes: IgG (up to 85%), IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.sted in order of their percentage in blood) into 5 classes: IgG (up to 85%), IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.ed in order of their percentage in blood) into 5 classes: IgG (up to 85%), IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.their percentage in blood) into 5 classes: IgG (up to 85%), IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.eir percentage in blood) into 5 classes: IgG (up to 85%), IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.r percentage in blood) into 5 classes: IgG (up to 85%), IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.ercentage in blood) into 5 classes: IgG (up to 85%), IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.centage in blood) into 5 classes: IgG (up to 85%), IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.ntage in blood) into 5 classes: IgG (up to 85%), IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.: IgG (up to 85%), IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.IgG (up to 85%), IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.G (up to 85%), IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.(up to 85%), IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.p to 85%), IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.to 85%), IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.%), IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person., IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.IgA (up to 15%), IgM (up to 10%), IgD (less 0.3%), IgE (less 0.003%) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.) where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.where capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.ere capital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.pital letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.tal letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.l letter designates the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.es the immunoglobulin class. IgG, IgD and IgE molecules are present as monomers, IgM - as pentamers; IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person. the immunoglobulin class. 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IgA molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person. molecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.olecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.ecules in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.es in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person. in blood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.ood are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.d are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.are monomers, and in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.nd in excreted liquids (lachrymal fluid, saliva and mucus) are dimers. 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Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.liva and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.va and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person. and mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.nd mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person. mucus) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.s) are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person. are dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.re dimers. Numerous possible combinations of L- and H-chains compose a diversity of AB in each person.e a diversity of AB in each person.a diversity of AB in each person.diversity of AB in each person.ity of AB in each person.y of AB in each person.of AB in each person.son.n.lass="">IgM synthesis is induced by primary Ag penetration in organism. The synthesis reaches maximum on 4-5th day and the titer decreases afterwards. IgM is constantly being synthesized in response to certain AG, e.g. bacterial filamental AG. Most AB against gram-negative bacteria belong to IgM class. Presence of IgM against a certain pathogenic Ag is indicative of an acute infectious process. IgM molecule is a pentamer: 5 subunits are joined by J-chain (J-joining) as a result IgM molecule acquires 10 AG-binding sites. IgM molecules opsonize, agglutinate, precipitate, lyse Ag containing structures, and activate complement system by classical pathway (one IgM molecule is capable of complement-mediated bacterial lysis).ss="">IgM synthesis is induced by primary Ag penetration in organism. The synthesis reaches maximum on 4-5th day and the titer decreases afterwards. IgM is constantly being synthesized in response to certain AG, e.g. bacterial filamental AG. Most AB against gram-negative bacteria belong to IgM class. Presence of IgM against a certain pathogenic Ag is indicative of an acute infectious process. IgM molecule is a pentamer: 5 subunits are joined by J-chain (J-joining) as a result IgM molecule acquires 10 AG-binding sites. IgM molecules opsonize, agglutinate, precipitate, lyse Ag containing structures, and activate complement system by classical pathway (one IgM molecule is capable of complement-mediated bacterial lysis).="">IgM synthesis is induced by primary Ag penetration in organism. The synthesis reaches maximum on 4-5th day and the titer decreases afterwards. IgM is constantly being synthesized in response to certain AG, e.g. bacterial filamental AG. Most AB against gram-negative bacteria belong to IgM class. Presence of IgM against a certain pathogenic Ag is indicative of an acute infectious process. IgM molecule is a pentamer: 5 subunits are joined by J-chain (J-joining) as a result IgM molecule acquires 10 AG-binding sites. IgM molecules opsonize, agglutinate, precipitate, lyse Ag containing structures, and activate complement system by classical pathway (one IgM molecule is capable of complement-mediated bacterial lysis).">IgM synthesis is induced by primary Ag penetration in organism. The synthesis reaches maximum on 4-5th day and the titer decreases afterwards. IgM is constantly being synthesized in response to certain AG, e.g. bacterial filamental AG. Most AB against gram-negative bacteria belong to IgM class. Presence of IgM against a certain pathogenic Ag is indicative of an acute infectious process. IgM molecule is a pentamer: 5 subunits are joined by J-chain (J-joining) as a result IgM molecule acquires 10 AG-binding sites. IgM molecules opsonize, agglutinate, precipitate, lyse Ag containing structures, and activate complement system by classical pathway (one IgM molecule is capable of complement-mediated bacterial lysis).IgM synthesis is induced by primary Ag penetration in organism. The synthesis reaches maximum on 4-5th day and the titer decreases afterwards. IgM is constantly being synthesized in response to certain AG, e.g. bacterial filamental AG. Most AB against gram-negative bacteria belong to IgM class. Presence of IgM against a certain pathogenic Ag is indicative of an acute infectious process. IgM molecule is a pentamer: 5 subunits are joined by J-chain (J-joining) as a result IgM molecule acquires 10 AG-binding sites. IgM molecules opsonize, agglutinate, precipitate, lyse Ag containing structures, and activate complement system by classical pathway (one IgM molecule is capable of complement-mediated bacterial lysis).M synthesis is induced by primary Ag penetration in organism. The synthesis reaches maximum on 4-5th day and the titer decreases afterwards. IgM is constantly being synthesized in response to certain AG, e.g. bacterial filamental AG. Most AB against gram-negative bacteria belong to IgM class. Presence of IgM against a certain pathogenic Ag is indicative of an acute infectious process. IgM molecule is a pentamer: 5 subunits are joined by J-chain (J-joining) as a result IgM molecule acquires 10 AG-binding sites. IgM molecules opsonize, agglutinate, precipitate, lyse Ag containing structures, and activate complement system by classical pathway (one IgM molecule is capable of complement-mediated bacterial lysis).synthesis is induced by primary Ag penetration in organism. The synthesis reaches maximum on 4-5th day and the titer decreases afterwards. IgM is constantly being synthesized in response to certain AG, e.g. bacterial filamental AG. Most AB against gram-negative bacteria belong to IgM class. Presence of IgM against a certain pathogenic Ag is indicative of an acute infectious process. IgM molecule is a pentamer: 5 subunits are joined by J-chain (J-joining) as a result IgM molecule acquires 10 AG-binding sites. IgM molecules opsonize, agglutinate, precipitate, lyse Ag containing structures, and activate complement system by classical pathway (one IgM molecule is capable of complement-mediated bacterial lysis).hesis is induced by primary Ag penetration in organism. The synthesis reaches maximum on 4-5th day and the titer decreases afterwards. IgM is constantly being synthesized in response to certain AG, e.g. bacterial filamental AG. Most AB against gram-negative bacteria belong to IgM class. Presence of IgM against a certain pathogenic Ag is indicative of an acute infectious process. IgM molecule is a pentamer: 5 subunits are joined by J-chain (J-joining) as a result IgM molecule acquires 10 AG-binding sites. IgM molecules opsonize, agglutinate, precipitate, lyse Ag containing structures, and activate complement system by classical pathway (one IgM molecule is capable of complement-mediated bacterial lysis).sis is induced by primary Ag penetration in organism. The synthesis reaches maximum on 4-5th day and the titer decreases afterwards. IgM is constantly being synthesized in response to certain AG, e.g. bacterial filamental AG. Most AB against gram-negative bacteria belong to IgM class. Presence of IgM against a certain pathogenic Ag is indicative of an acute infectious process. IgM molecule is a pentamer: 5 subunits are joined by J-chain (J-joining) as a result IgM molecule acquires 10 AG-binding sites. IgM molecules opsonize, agglutinate, precipitate, lyse Ag containing structures, and activate complement system by classical pathway (one IgM molecule is capable of complement-mediated bacterial lysis).s is induced by primary Ag penetration in organism. The synthesis reaches maximum on 4-5th day and the titer decreases afterwards. IgM is constantly being synthesized in response to certain AG, e.g. bacterial filamental AG. Most AB against gram-negative bacteria belong to IgM class. Presence of IgM against a certain pathogenic Ag is indicative of an acute infectious process. IgM molecule is a pentamer: 5 subunits are joined by J-chain (J-joining) as a result IgM molecule acquires 10 AG-binding sites. IgM molecules opsonize, agglutinate, precipitate, lyse Ag containing structures, and activate complement system by classical pathway (one IgM molecule is capable of complement-mediated bacterial lysis). induced by primary Ag penetration in organism. The synthesis reaches maximum on 4-5th day and the titer decreases afterwards. IgM is constantly being synthesized in response to certain AG, e.g. bacterial filamental AG. Most AB against gram-negative bacteria belong to IgM class. Presence of IgM against a certain pathogenic Ag is indicative of an acute infectious process. IgM molecule is a pentamer: 5 subunits are joined by J-chain (J-joining) as a result IgM molecule acquires 10 AG-binding sites. IgM molecules opsonize, agglutinate, precipitate, lyse Ag containing structures, and activate complement system by classical pathway (one IgM molecule is capable of complement-mediated bacterial lysis).nduced by primary Ag penetration in organism. The synthesis reaches maximum on 4-5th day and the titer decreases afterwards. IgM is constantly being synthesized in response to certain AG, e.g. bacterial filamental AG. Most AB against gram-negative bacteria belong to IgM class. Presence of IgM against a certain pathogenic Ag is indicative of an acute infectious process. IgM molecule is a pentamer: 5 subunits are joined by J-chain (J-joining) as a result IgM molecule acquires 10 AG-binding sites. IgM molecules opsonize, agglutinate, precipitate, lyse Ag containing structures, and activate complement system by classical pathway (one IgM molecule is capable of complement-mediated bacterial lysis). by primary Ag penetration in organism. The synthesis reaches maximum on 4-5th day and the titer decreases afterwards. IgM is constantly being synthesized in response to certain AG, e.g. bacterial filamental AG. Most AB against gram-negative bacteria belong to IgM class. Presence of IgM against a certain pathogenic Ag is indicative of an acute infectious process. IgM molecule is a pentamer: 5 subunits are joined by J-chain (J-joining) as a result IgM molecule acquires 10 AG-binding sites. IgM molecules opsonize, agglutinate, precipitate, lyse Ag containing structures, and activate complement system by classical pathway (one IgM molecule is capable of complement-mediated bacterial lysis).y primary Ag penetration in organism. The synthesis reaches maximum on 4-5th day and the titer decreases afterwards. IgM is constantly being synthesized in response to certain AG, e.g. bacterial filamental AG. Most AB against gram-negative bacteria belong to IgM class. Presence of IgM against a certain pathogenic Ag is indicative of an acute infectious process. IgM molecule is a pentamer: 5 subunits are joined by J-chain (J-joining) as a result IgM molecule acquires 10 AG-binding sites. IgM molecules opsonize, agglutinate, precipitate, lyse Ag containing structures, and activate complement system by classical pathway (one IgM molecule is capable of complement-mediated bacterial lysis).primary Ag penetration in organism. The synthesis reaches maximum on 4-5th day and the titer decreases afterwards. IgM is constantly being synthesized in response to certain AG, e.g. bacterial filamental AG. Most AB against gram-negative bacteria belong to IgM class. Presence of IgM against a certain pathogenic Ag is indicative of an acute infectious process. IgM molecule is a pentamer: 5 subunits are joined by J-chain (J-joining) as a result IgM molecule acquires 10 AG-binding sites. IgM molecules opsonize, agglutinate, precipitate, lyse Ag containing structures, and activate complement system by classical pathway (one IgM molecule is capable of complement-mediated bacterial lysis).tration in organism. The synthesis reaches maximum on 4-5th day and the titer decreases afterwards. IgM is constantly being synthesized in response to certain AG, e.g. bacterial filamental AG. Most AB against gram-negative bacteria belong to IgM class. Presence of IgM against a certain pathogenic Ag is indicative of an acute infectious process. IgM molecule is a pentamer: 5 subunits are joined by J-chain (J-joining) as a result IgM molecule acquires 10 AG-binding sites. IgM molecules opsonize, agglutinate, precipitate, lyse Ag containing structures, and activate complement system by classical pathway (one IgM molecule is capable of complement-mediated bacterial lysis).ation in organism. The synthesis reaches maximum on 4-5th day and the titer decreases afterwards. IgM is constantly being synthesized in response to certain AG, e.g. bacterial filamental AG. Most AB against gram-negative bacteria belong to IgM class. Presence of IgM against a certain pathogenic Ag is indicative of an acute infectious process. IgM molecule is a pentamer: 5 subunits are joined by J-chain (J-joining) as a result IgM molecule acquires 10 AG-binding sites. IgM molecules opsonize, agglutinate, precipitate, lyse Ag containing structures, and activate complement system by classical pathway (one IgM molecule is capable of complement-mediated bacterial lysis).ion in organism. The synthesis reaches maximum on 4-5th day and the titer decreases afterwards. IgM is constantly being synthesized in response to certain AG, e.g. bacterial filamental AG. Most AB against gram-negative bacteria belong to IgM class. Presence of IgM against a certain pathogenic Ag is indicative of an acute infectious process. IgM molecule is a pentamer: 5 subunits are joined by J-chain (J-joining) as a result IgM molecule acquires 10 AG-binding sites. IgM molecules opsonize, agglutinate, precipitate, lyse Ag containing structures, and activate complement system by classical pathway (one IgM molecule is capable of complement-mediated bacterial lysis). in organism. The synthesis reaches maximum on 4-5th day and the titer decreases afterwards. IgM is constantly being synthesized in response to certain AG, e.g. bacterial filamental AG. Most AB against gram-negative bacteria belong to IgM class. Presence of IgM against a certain pathogenic Ag is indicative of an acute infectious process. IgM molecule is a pentamer: 5 subunits are joined by J-chain (J-joining) as a result IgM molecule acquires 10 AG-binding sites. IgM molecules opsonize, agglutinate, precipitate, lyse Ag containing structures, and activate complement system by classical pathway (one IgM molecule is capable of complement-mediated bacterial lysis).n organism. The synthesis reaches maximum on 4-5th day and the titer decreases afterwards. IgM is constantly being synthesized in response to certain AG, e.g. bacterial filamental AG. Most AB against gram-negative bacteria belong to IgM class. Presence of IgM against a certain pathogenic Ag is indicative of an acute infectious process. IgM molecule is a pentamer: 5 subunits are joined by J-chain (J-joining) as a result IgM molecule acquires 10 AG-binding sites. IgM molecules opsonize, agglutinate, precipitate, lyse Ag containing structures, and activate complement system by classical pathway (one IgM molecule is capable of complement-mediated bacterial lysis).organism. The synthesis reaches maximum on 4-5th day and the titer decreases afterwards. IgM is constantly being synthesized in response to certain AG, e.g. bacterial filamental AG. Most AB against gram-negative bacteria belong to IgM class. Presence of IgM against a certain pathogenic Ag is indicative of an acute infectious process. IgM molecule is a pentamer: 5 subunits are joined by J-chain (J-joining) as a result IgM molecule acquires 10 AG-binding sites. IgM molecules opsonize, agglutinate, precipitate, lyse Ag containing structures, and activate complement system by classical pathway (one IgM molecule is capable of complement-mediated bacterial lysis).s maximum on 4-5th day and the titer decreases afterwards. IgM is constantly being synthesized in response to certain AG, e.g. bacterial filamental AG. Most AB against gram-negative bacteria belong to IgM class. Presence of IgM against a certain pathogenic Ag is indicative of an acute infectious process. IgM molecule is a pentamer: 5 subunits are joined by J-chain (J-joining) as a result IgM molecule acquires 10 AG-binding sites. IgM molecules opsonize, agglutinate, precipitate, lyse Ag containing structures, and activate complement system by classical pathway (one IgM molecule is capable of complement-mediated bacterial lysis).maximum on 4-5th day and the titer decreases afterwards. IgM is constantly being synthesized in response to certain AG, e.g. bacterial filamental AG. Most AB against gram-negative bacteria belong to IgM class. Presence of IgM against a certain pathogenic Ag is indicative of an acute infectious process. IgM molecule is a pentamer: 5 subunits are joined by J-chain (J-joining) as a result IgM molecule acquires 10 AG-binding sites. IgM molecules opsonize, agglutinate, precipitate, lyse Ag containing structures, and activate complement system by classical pathway (one IgM molecule is capable of complement-mediated bacterial lysis).ximum on 4-5th day and the titer decreases afterwards. IgM is constantly being synthesized in response to certain AG, e.g. bacterial filamental AG. Most AB against gram-negative bacteria belong to IgM class. Presence of IgM against a certain pathogenic Ag is indicative of an acute infectious process. IgM molecule is a pentamer: 5 subunits are joined by J-chain (J-joining) as a result IgM molecule acquires 10 AG-binding sites. IgM molecules opsonize, agglutinate, precipitate, lyse Ag containing structures, and activate complement system by classical pathway (one IgM molecule is capable of complement-mediated bacterial lysis).mum on 4-5th day and the titer decreases afterwards. IgM is constantly being synthesized in response to certain AG, e.g. bacterial filamental AG. Most AB against gram-negative bacteria belong to IgM class. Presence of IgM against a certain pathogenic Ag is indicative of an acute infectious process. IgM molecule is a pentamer: 5 subunits are joined by J-chain (J-joining) as a result IgM molecule acquires 10 AG-binding sites. IgM molecules opsonize, agglutinate, precipitate, lyse Ag containing structures, and activate complement system by classical pathway (one IgM molecule is capable of complement-mediated bacterial lysis).m on 4-5th day and the titer decreases afterwards. IgM is constantly being synthesized in response to certain AG, e.g. bacterial filamental AG. Most AB against gram-negative bacteria belong to IgM class. Presence of IgM against a certain pathogenic Ag is indicative of an acute infectious process. IgM molecule is a pentamer: 5 subunits are joined by J-chain (J-joining) as a result IgM molecule acquires 10 AG-binding sites. IgM molecules opsonize, agglutinate, precipitate, lyse Ag containing structures, and activate complement system by classical pathway (one IgM molecule is capable of complement-mediated bacterial lysis).on 4-5th day and the titer decreases afterwards. IgM is constantly being synthesized in response to certain AG, e.g. bacterial filamental AG. Most AB against gram-negative bacteria belong to IgM class. Presence of IgM against a certain pathogenic Ag is indicative of an acute infectious process. IgM molecule is a pentamer: 5 subunits are joined by J-chain (J-joining) as a result IgM molecule acquires 10 AG-binding sites. IgM molecules opsonize, agglutinate, precipitate, lyse Ag containing structures, and activate complement system by classical pathway (one IgM molecule is capable of complement-mediated bacterial lysis).5th day and the titer decreases afterwards. IgM is constantly being synthesized in response to certain AG, e.g. bacterial filamental AG. Most AB against gram-negative bacteria belong to IgM class. Presence of IgM against a certain pathogenic Ag is indicative of an acute infectious process. IgM molecule is a pentamer: 5 subunits are joined by J-chain (J-joining) as a result IgM molecule acquires 10 AG-binding sites. IgM molecules opsonize, agglutinate, precipitate, lyse Ag containing structures, and activate complement system by classical pathway (one IgM molecule is capable of complement-mediated bacterial lysis).h day and the titer decreases afterwards. IgM is constantly being synthesized in response to certain AG, e.g. bacterial filamental AG. Most AB against gram-negative bacteria belong to IgM class. Presence of IgM against a certain pathogenic Ag is indicative of an acute infectious process. IgM molecule is a pentamer: 5 subunits are joined by J-chain (J-joining) as a result IgM molecule acquires 10 AG-binding sites. IgM molecules opsonize, agglutinate, precipitate, lyse Ag containing structures, and activate complement system by classical pathway (one IgM molecule is capable of complement-mediated bacterial lysis).day and the titer decreases afterwards. IgM is constantly being synthesized in response to certain AG, e.g. bacterial filamental AG. Most AB against gram-negative bacteria belong to IgM class. Presence of IgM against a certain pathogenic Ag is indicative of an acute infectious process. IgM molecule is a pentamer: 5 subunits are joined by J-chain (J-joining) as a result IgM molecule acquires 10 AG-binding sites. IgM molecules opsonize, agglutinate, precipitate, lyse Ag containing structures, and activate complement system by classical pathway (one IgM molecule is capable of complement-mediated bacterial lysis).thesized in response to certain AG, e.g. bacterial filamental AG. Most AB against gram-negative bacteria belong to IgM class. Presence of IgM against a certain pathogenic Ag is indicative of an acute infectious process. IgM molecule is a pentamer: 5 subunits are joined by J-chain (J-joining) as a result IgM molecule acquires 10 AG-binding sites. IgM molecules opsonize, agglutinate, precipitate, lyse Ag containing structures, and activate complement system by classical pathway (one IgM molecule is capable of complement-mediated bacterial lysis).esized in response to certain AG, e.g. bacterial filamental AG. Most AB against gram-negative bacteria belong to IgM class. Presence of IgM against a certain pathogenic Ag is indicative of an acute infectious process. IgM molecule is a pentamer: 5 subunits are joined by J-chain (J-joining) as a result IgM molecule acquires 10 AG-binding sites. IgM molecules opsonize, agglutinate, precipitate, lyse Ag containing structures, and activate complement system by classical pathway (one IgM molecule is capable of complement-mediated bacterial lysis).ized in response to certain AG, e.g. bacterial filamental AG. Most AB against gram-negative bacteria belong to IgM class. Presence of IgM against a certain pathogenic Ag is indicative of an acute infectious process. IgM molecule is a pentamer: 5 subunits are joined by J-chain (J-joining) as a result IgM molecule acquires 10 AG-binding sites. IgM molecules opsonize, agglutinate, precipitate, lyse Ag containing structures, and activate complement system by classical pathway (one IgM molecule is capable of complement-mediated bacterial lysis).n response to certain AG, e.g. bacterial filamental AG. Most AB against gram-negative bacteria belong to IgM class. Presence of IgM against a certain pathogenic Ag is indicative of an acute infectious process. IgM molecule is a pentamer: 5 subunits are joined by J-chain (J-joining) as a result IgM molecule acquires 10 AG-binding sites. IgM molecules opsonize, agglutinate, precipitate, lyse Ag containing structures, and activate complement system by classical pathway (one IgM molecule is capable of complement-mediated bacterial lysis).response to certain AG, e.g. bacterial filamental AG. Most AB against gram-negative bacteria belong to IgM class. Presence of IgM against a certain pathogenic Ag is indicative of an acute infectious process. IgM molecule is a pentamer: 5 subunits are joined by J-chain (J-joining) as a result IgM molecule acquires 10 AG-binding sites. IgM molecules opsonize, agglutinate, precipitate, lyse Ag containing structures, and activate complement system by classical pathway (one IgM molecule is capable of complement-mediated bacterial lysis).sponse to certain AG, e.g. bacterial filamental AG. Most AB against gram-negative bacteria belong to IgM class. Presence of IgM against a certain pathogenic Ag is indicative of an acute infectious process. IgM molecule is a pentamer: 5 subunits are joined by J-chain (J-joining) as a result IgM molecule acquires 10 AG-binding sites. IgM molecules opsonize, agglutinate, precipitate, lyse Ag containing structures, and activate complement system by classical pathway (one IgM molecule is capable of complement-mediated bacterial lysis). AG, e.g. bacterial filamental AG. Most AB against gram-negative bacteria belong to IgM class. Presence of IgM against a certain pathogenic Ag is indicative of an acute infectious process. IgM molecule is a pentamer: 5 subunits are joined by J-chain (J-joining) as a result IgM molecule acquires 10 AG-binding sites. IgM molecules opsonize, agglutinate, precipitate, lyse Ag containing structures, and activate complement system by classical pathway (one IgM molecule is capable of complement-mediated bacterial lysis).G, e.g. bacterial filamental AG. Most AB against gram-negative bacteria belong to IgM class. Presence of IgM against a certain pathogenic Ag is indicative of an acute infectious process. IgM molecule is a pentamer: 5 subunits are joined by J-chain (J-joining) as a result IgM molecule acquires 10 AG-binding sites. IgM molecules opsonize, agglutinate, precipitate, lyse Ag containing structures, and activate complement system by classical pathway (one IgM molecule is capable of complement-mediated bacterial lysis). e.g. bacterial filamental AG. Most AB against gram-negative bacteria belong to IgM class. Presence of IgM against a certain pathogenic Ag is indicative of an acute infectious process. IgM molecule is a pentamer: 5 subunits are joined by J-chain (J-joining) as a result IgM molecule acquires 10 AG-binding sites. IgM molecules opsonize, agglutinate, precipitate, lyse Ag containing structures, and activate complement system by classical pathway (one IgM molecule is capable of complement-mediated bacterial lysis).negative bacteria belong to IgM class. Presence of IgM against a certain pathogenic Ag is indicative of an acute infectious process. IgM molecule is a pentamer: 5 subunits are joined by J-chain (J-joining) as a result IgM molecule acquires 10 AG-binding sites. IgM molecules opsonize, agglutinate, precipitate, lyse Ag containing structures, and activate complement system by classical pathway (one IgM molecule is capable of complement-mediated bacterial lysis).gative bacteria belong to IgM class. Presence of IgM against a certain pathogenic Ag is indicative of an acute infectious process. IgM molecule is a pentamer: 5 subunits are joined by J-chain (J-joining) as a result IgM molecule acquires 10 AG-binding sites. IgM molecules opsonize, agglutinate, precipitate, lyse Ag containing structures, and activate complement system by classical pathway (one IgM molecule is capable of complement-mediated bacterial lysis).tive bacteria belong to IgM class. Presence of IgM against a certain pathogenic Ag is indicative of an acute infectious process. IgM molecule is a pentamer: 5 subunits are joined by J-chain (J-joining) as a result IgM molecule acquires 10 AG-binding sites. IgM molecules opsonize, agglutinate, precipitate, lyse Ag containing structures, and activate complement system by classical pathway (one IgM molecule is capable of complement-mediated bacterial lysis).ve bacteria belong to IgM class. Presence of IgM against a certain pathogenic Ag is indicative of an acute infectious process. IgM molecule is a pentamer: 5 subunits are joined by J-chain (J-joining) as a result IgM molecule acquires 10 AG-binding sites. IgM molecules opsonize, agglutinate, precipitate, lyse Ag containing structures, and activate complement system by classical pathway (one IgM molecule is capable of complement-mediated bacterial lysis). bacteria belong to IgM class. Presence of IgM against a certain pathogenic Ag is indicative of an acute infectious process. IgM molecule is a pentamer: 5 subunits are joined by J-chain (J-joining) as a result IgM molecule acquires 10 AG-binding sites. IgM molecules opsonize, agglutinate, precipitate, lyse Ag containing structures, and activate complement system by classical pathway (one IgM molecule is capable of complement-mediated bacterial lysis).acteria belong to IgM class. Presence of IgM against a certain pathogenic Ag is indicative of an acute infectious process. IgM molecule is a pentamer: 5 subunits are joined by J-chain (J-joining) as a result IgM molecule acquires 10 AG-binding sites. IgM molecules opsonize, agglutinate, precipitate, lyse Ag containing structures, and activate complement system by classical pathway (one IgM molecule is capable of complement-mediated bacterial lysis).teria belong to IgM class. Presence of IgM against a certain pathogenic Ag is indicative of an acute infectious process. IgM molecule is a pentamer: 5 subunits are joined by J-chain (J-joining) as a result IgM molecule acquires 10 AG-binding sites. IgM molecules opsonize, agglutinate, precipitate, lyse Ag containing structures, and activate complement system by classical pathway (one IgM molecule is capable of complement-mediated bacterial lysis).a belong to IgM class. Presence of IgM against a certain pathogenic Ag is indicative of an acute infectious process. IgM molecule is a pentamer: 5 subunits are joined by J-chain (J-joining) as a result IgM molecule acquires 10 AG-binding sites. IgM molecules opsonize, agglutinate, precipitate, lyse Ag containing structures, and activate complement system by classical pathway (one IgM molecule is capable of complement-mediated bacterial lysis).belong to IgM class. Presence of IgM against a certain pathogenic Ag is indicative of an acute infectious process. IgM molecule is a pentamer: 5 subunits are joined by J-chain (J-joining) as a result IgM molecule acquires 10 AG-binding sites. IgM molecules opsonize, agglutinate, precipitate, lyse Ag containing structures, and activate complement system by classical pathway (one IgM molecule is capable of complement-mediated bacterial lysis).long to IgM class. Presence of IgM against a certain pathogenic Ag is indicative of an acute infectious process. IgM molecule is a pentamer: 5 subunits are joined by J-chain (J-joining) as a result IgM molecule acquires 10 AG-binding sites. IgM molecules opsonize, agglutinate, precipitate, lyse Ag containing structures, and activate complement system by classical pathway (one IgM molecule is capable of complement-mediated bacterial lysis). to IgM class. Presence of IgM against a certain pathogenic Ag is indicative of an acute infectious process. IgM molecule is a pentamer: 5 subunits are joined by J-chain (J-joining) as a result IgM molecule acquires 10 AG-binding sites. IgM molecules opsonize, agglutinate, precipitate, lyse Ag containing structures, and activate complement system by classical pathway (one IgM molecule is capable of complement-mediated bacterial lysis).o IgM class. Presence of IgM against a certain pathogenic Ag is indicative of an acute infectious process. IgM molecule is a pentamer: 5 subunits are joined by J-chain (J-joining) as a result IgM molecule acquires 10 AG-binding sites. IgM molecules opsonize, agglutinate, precipitate, lyse Ag containing structures, and activate complement system by classical pathway (one IgM molecule is capable of complement-mediated bacterial lysis).class. Presence of IgM against a certain pathogenic Ag is indicative of an acute infectious process. IgM molecule is a pentamer: 5 subunits are joined by J-chain (J-joining) as a result IgM molecule acquires 10 AG-binding sites. IgM molecules opsonize, agglutinate, precipitate, lyse Ag containing structures, and activate complement system by classical pathway (one IgM molecule is capable of complement-mediated bacterial lysis).ass. Presence of IgM against a certain pathogenic Ag is indicative of an acute infectious process. IgM molecule is a pentamer: 5 subunits are joined by J-chain (J-joining) as a result IgM molecule acquires 10 AG-binding sites. IgM molecules opsonize, agglutinate, precipitate, lyse Ag containing structures, and activate complement system by classical pathway (one IgM molecule is capable of complement-mediated bacterial lysis).s. Presence of IgM against a certain pathogenic Ag is indicative of an acute infectious process. IgM molecule is a pentamer: 5 subunits are joined by J-chain (J-joining) as a result IgM molecule acquires 10 AG-binding sites. IgM molecules opsonize, agglutinate, precipitate, lyse Ag containing structures, and activate complement system by classical pathway (one IgM molecule is capable of complement-mediated bacterial lysis).IgM against a certain pathogenic Ag is indicative of an acute infectious process. IgM molecule is a pentamer: 5 subunits are joined by J-chain (J-joining) as a result IgM molecule acquires 10 AG-binding sites. IgM molecules opsonize, agglutinate, precipitate, lyse Ag containing structures, and activate complement system by classical pathway (one IgM molecule is capable of complement-mediated bacterial lysis).M against a certain pathogenic Ag is indicative of an acute infectious process. IgM molecule is a pentamer: 5 subunits are joined by J-chain (J-joining) as a result IgM molecule acquires 10 AG-binding sites. IgM molecules opsonize, agglutinate, precipitate, lyse Ag containing structures, and activate complement system by classical pathway (one IgM molecule is capable of complement-mediated bacterial lysis).against a certain pathogenic Ag is indicative of an acute infectious process. IgM molecule is a pentamer: 5 subunits are joined by J-chain (J-joining) as a result IgM molecule acquires 10 AG-binding sites. IgM molecules opsonize, agglutinate, precipitate, lyse Ag containing structures, and activate complement system by classical pathway (one IgM molecule is capable of complement-mediated bacterial lysis).inst a certain pathogenic Ag is indicative of an acute infectious process. IgM molecule is a pentamer: 5 subunits are joined by J-chain (J-joining) as a result IgM molecule acquires 10 AG-binding sites. IgM molecules opsonize, agglutinate, precipitate, lyse Ag containing structures, and activate complement system by classical pathway (one IgM molecule is capable of complement-mediated bacterial lysis).st a certain pathogenic Ag is indicative of an acute infectious process. IgM molecule is a pentamer: 5 subunits are joined by J-chain (J-joining) as a result IgM molecule acquires 10 AG-binding sites. IgM molecules opsonize, agglutinate, precipitate, lyse Ag containing structures, and activate complement system by classical pathway (one IgM molecule is capable of complement-mediated bacterial lysis). a certain pathogenic Ag is indicative of an acute infectious process. IgM molecule is a pentamer: 5 subunits are joined by J-chain (J-joining) as a result IgM molecule acquires 10 AG-binding sites. IgM molecules opsonize, agglutinate, precipitate, lyse Ag containing structures, and activate complement system by classical pathway (one IgM molecule is capable of complement-mediated bacterial lysis).dicative of an acute infectious process. IgM molecule is a pentamer: 5 subunits are joined by J-chain (J-joining) as a result IgM molecule acquires 10 AG-binding sites. IgM molecules opsonize, agglutinate, precipitate, lyse Ag containing structures, and activate complement system by classical pathway (one IgM molecule is capable of complement-mediated bacterial lysis).cative of an acute infectious process. IgM molecule is a pentamer: 5 subunits are joined by J-chain (J-joining) as a result IgM molecule acquires 10 AG-binding sites. IgM molecules opsonize, agglutinate, precipitate, lyse Ag containing structures, and activate complement system by classical pathway (one IgM molecule is capable of complement-mediated bacterial lysis).tive of an acute infectious process. IgM molecule is a pentamer: 5 subunits are joined by J-chain (J-joining) as a result IgM molecule acquires 10 AG-binding sites. IgM molecules opsonize, agglutinate, precipitate, lyse Ag containing structures, and activate complement system by classical pathway (one IgM molecule is capable of complement-mediated bacterial lysis).ve of an acute infectious process. IgM molecule is a pentamer: 5 subunits are joined by J-chain (J-joining) as a result IgM molecule acquires 10 AG-binding sites. IgM molecules opsonize, agglutinate, precipitate, lyse Ag containing structures, and activate complement system by classical pathway (one IgM molecule is capable of complement-mediated bacterial lysis). of an acute infectious process. IgM molecule is a pentamer: 5 subunits are joined by J-chain (J-joining) as a result IgM molecule acquires 10 AG-binding sites. IgM molecules opsonize, agglutinate, precipitate, lyse Ag containing structures, and activate complement system by classical pathway (one IgM molecule is capable of complement-mediated bacterial lysis).f an acute infectious process. IgM molecule is a pentamer: 5 subunits are joined by J-chain (J-joining) as a result IgM molecule acquires 10 AG-binding sites. IgM molecules opsonize, agglutinate, precipitate, lyse Ag containing structures, and activate complement system by classical pathway (one IgM molecule is capable of complement-mediated bacterial lysis).acute infectious process. IgM molecule is a pentamer: 5 subunits are joined by J-chain (J-joining) as a result IgM molecule acquires 10 AG-binding sites. IgM molecules opsonize, agglutinate, precipitate, lyse Ag containing structures, and activate complement system by classical pathway (one IgM molecule is capable of complement-mediated bacterial lysis).ute infectious process. IgM molecule is a pentamer: 5 subunits are joined by J-chain (J-joining) as a result IgM molecule acquires 10 AG-binding sites. IgM molecules opsonize, agglutinate, precipitate, lyse Ag containing structures, and activate complement system by classical pathway (one IgM molecule is capable of complement-mediated bacterial lysis).e infectious process. IgM molecule is a pentamer: 5 subunits are joined by J-chain (J-joining) as a result IgM molecule acquires 10 AG-binding sites. IgM molecules opsonize, agglutinate, precipitate, lyse Ag containing structures, and activate complement system by classical pathway (one IgM molecule is capable of complement-mediated bacterial lysis).ined by J-chain (J-joining) as a result IgM molecule acquires 10 AG-binding sites. IgM molecules opsonize, agglutinate, precipitate, lyse Ag containing structures, and activate complement system by classical pathway (one IgM molecule is capable of complement-mediated bacterial lysis).ed by J-chain (J-joining) as a result IgM molecule acquires 10 AG-binding sites. IgM molecules opsonize, agglutinate, precipitate, lyse Ag containing structures, and activate complement system by classical pathway (one IgM molecule is capable of complement-mediated bacterial lysis). by J-chain (J-joining) as a result IgM molecule acquires 10 AG-binding sites. IgM molecules opsonize, agglutinate, precipitate, lyse Ag containing structures, and activate complement system by classical pathway (one IgM molecule is capable of complement-mediated bacterial lysis).chain (J-joining) as a result IgM molecule acquires 10 AG-binding sites. IgM molecules opsonize, agglutinate, precipitate, lyse Ag containing structures, and activate complement system by classical pathway (one IgM molecule is capable of complement-mediated bacterial lysis).ain (J-joining) as a result IgM molecule acquires 10 AG-binding sites. IgM molecules opsonize, agglutinate, precipitate, lyse Ag containing structures, and activate complement system by classical pathway (one IgM molecule is capable of complement-mediated bacterial lysis).n (J-joining) as a result IgM molecule acquires 10 AG-binding sites. IgM molecules opsonize, agglutinate, precipitate, lyse Ag containing structures, and activate complement system by classical pathway (one IgM molecule is capable of complement-mediated bacterial lysis).a result IgM molecule acquires 10 AG-binding sites. IgM molecules opsonize, agglutinate, precipitate, lyse Ag containing structures, and activate complement system by classical pathway (one IgM molecule is capable of complement-mediated bacterial lysis).result IgM molecule acquires 10 AG-binding sites. IgM molecules opsonize, agglutinate, precipitate, lyse Ag containing structures, and activate complement system by classical pathway (one IgM molecule is capable of complement-mediated bacterial lysis).sult IgM molecule acquires 10 AG-binding sites. IgM molecules opsonize, agglutinate, precipitate, lyse Ag containing structures, and activate complement system by classical pathway (one IgM molecule is capable of complement-mediated bacterial lysis). �АНТ СТУДЕНТА"

Электронная библиотечная система "Консультант студента"

Россия, Москва, ул.Садовническая, д. 11, стр.12.