Mouse Monoclonal ABO antibody. Carrier free. Suitable for Flow Cyt and reacts with Human samples. Cited in 2 publications.
Constituents: Tissue culture supernatant
Flow Cyt | |
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Human | Tested |
Species | Dilution info | Notes |
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Species Human | Dilution info - | Notes - |
This protein is the basis of the ABO blood group system. The histo-blood group ABO involves three carbohydrate antigens: A, B, and H. A, B, and AB individuals express a glycosyltransferase activity that converts the H antigen to the A antigen (by addition of UDP-GalNAc) or to the B antigen (by addition of UDP-Gal), whereas O individuals lack such activity. Glycosyltransferase that catalyzes the transfer of carbohydrates to H antigen, forming the antigenic structures of the ABO blood group.
Histo-blood group ABO system transferase, Fucosylglycoprotein 3-alpha-galactosyltransferase, Fucosylglycoprotein alpha-N-acetylgalactosaminyltransferase, Glycoprotein-fucosylgalactoside alpha-N-acetylgalactosaminyltransferase, Glycoprotein-fucosylgalactoside alpha-galactosyltransferase, Histo-blood group A transferase, Histo-blood group B transferase, NAGAT, A transferase, B transferase, ABO
Mouse Monoclonal ABO antibody. Carrier free. Suitable for Flow Cyt and reacts with Human samples. Cited in 2 publications.
Constituents: Tissue culture supernatant
Studies with specific oligosaccharides showed that this antibody detects A and H antigens with chain types 3 and 4. This antibody does not react with A disaccharide, A trisaccharide, A type 1, A type 2 or ALe b. This antibody reacts with normal and malignant tissue sections from donors with blood group A. It does not react with normal tissue sections from donors with blood group B and 0 but it does react specifically with malignant tissues.
Concentrated by ultrafiltration (100 kDa cut-off). Actual immunoglobulin concentration not determined.
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Blood Group A B and H antigens are carbohydrate molecules present on the surface of red blood cells. Also known as ABO blood group antigens they are a part of glycoproteins and glycolipids. Each of these antigens has a distinct oligosaccharide structure with the H antigen serving as the precursor to A and B antigens. The molecular mass varies as these antigens are part of larger glycoproteins. These antigens primarily express themselves on red blood cells but also appear on various epithelial and endothelial cells.
A B and H antigens significantly determine individuals' blood type whether it is A B AB or O. They do not form part of a complex but instead result from specific enzyme activity encoded by ABO genes. Glycosyltransferase enzymes modify the H antigen to form A or B antigens through the addition of monosaccharides. The presence or absence of these antigens results in corresponding antibodies against them in the plasma known as blood type antibodies or anti-A and anti-B antibodies important in transfusion medicine.
A B and H antigen biosynthesis involves glycosylation pathways where specific transferases act on precursor substances. In the glycosylation pathway proteins like fucosyltransferase are closely related contributing to forming the H antigen from the precursor glycoproteins. These pathways illustrate how genetic variations lead to different glycan structures establishing the basis for various blood types and their related antibodies such as anti-A anti-B and the lack thereof in O type.
Differences in A B and H antigens are particularly relevant in transfusion reactions and hemolytic diseases of the newborn. Incompatible blood transfusions can lead to immune responses when antibodies target antigens present on donor cells. Disorders such as Bombay phenotype arise when individuals lack H antigen altogether complicating blood transfusions since they can produce antibodies against A B and H antigens. Related proteins in these conditions include those involved in immune response and complement pathways which get activated during antigen-antibody reactions.
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Separation of human erythrocytes from blood group A donor (red-filled) from erythrocytes from blood group 0 donor (black-dashed) in flow cytometry analysis (surface staining) of human peripheral whole blood samples using ab2523.
Flow cytometry surface staining pattern of human peripheral whole blood from group A donor stained using ab2523.
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