Blood Group A1 and A2 antigen inhibitors are a specialized category of biochemical agents designed to target and inhibit the function of specific antigens associated with the ABO blood group system. Within this system, the A1 and A2 antigens are subtypes of the A antigen, differing slightly in their structural composition and the density of antigenic sites on the red blood cell surface. The A1 antigen is more prevalent and has a higher number of antigenic sites compared to the A2 antigen. Inhibitors targeting these antigens are molecules that can specifically bind to the unique molecular structures of the A1 or A2 antigens. By binding to these antigens, the inhibitors can interfere with the normal antigen-antibody interactions that define the blood group properties of these cells.
The development and characterization of Blood Group A1, A2 antigen inhibitors involve understanding the biochemical and structural nuances of the ABO blood group antigens. The A1 and A2 antigens are complex carbohydrate structures that are attached to glycoproteins and glycolipids on the red blood cell membrane. These structures are synthesized by specific glycosyltransferases that add sugars to a precursor substance, H antigen, to form the A antigen. The A1 and A2 antigens differ in their terminal sugars and the linkages between these sugars, which confer unique three-dimensional structures. Inhibitors of these antigens are often complex molecules that mimic these terminal sugar structures to competitively inhibit the binding sites of natural ligands. Precision in designing these inhibitors is critical because the antigenic determinants of the A1 and A2 antigens must be specifically recognized and blocked without affecting other components of the cells or other similar antigens.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Tunicamycin | 11089-65-9 | sc-3506A sc-3506 | 5 mg 10 mg | $169.00 $299.00 | 66 | |
Inhibits N-linked glycosylation by blocking the transfer of N-acetylglucosamine to dolichol phosphate. | ||||||
Swainsonine | 72741-87-8 | sc-201362 sc-201362C sc-201362A sc-201362D sc-201362B | 1 mg 2 mg 5 mg 10 mg 25 mg | $135.00 $246.00 $619.00 $799.00 $1796.00 | 6 | |
Inhibits Golgi alpha-mannosidase II, interfering with the trimming of mannose residues in N-glycans. | ||||||
Brefeldin A | 20350-15-6 | sc-200861C sc-200861 sc-200861A sc-200861B | 1 mg 5 mg 25 mg 100 mg | $30.00 $52.00 $122.00 $367.00 | 25 | |
Disrupts transport within the Golgi apparatus, leading to a failure in the processing and expression of glycoproteins. | ||||||
Deoxynojirimycin | 19130-96-2 | sc-201369 sc-201369A | 1 mg 5 mg | $72.00 $142.00 | ||
Inhibits alpha-glucosidases I and II, enzymes involved in the folding of N-linked glycoproteins. | ||||||
Castanospermine | 79831-76-8 | sc-201358 sc-201358A | 100 mg 500 mg | $180.00 $620.00 | 10 | |
Inhibits glucosidase, which can prevent proper glycoprotein folding and indirectly affect antigen expression. | ||||||
Ceftriaxone, Disodium Salt, Hemiheptahydrate | 104376-79-6 | sc-211050 sc-211050A | 1 g 5 g | $175.00 $440.00 | 1 | |
Inhibits mannosidase, disrupting the processing of N-linked oligosaccharides in glycoproteins. | ||||||
Kifunensine | 109944-15-2 | sc-201364 sc-201364A sc-201364B sc-201364C | 1 mg 5 mg 10 mg 100 mg | $132.00 $529.00 $1005.00 $6125.00 | 25 | |
Inhibits mannosidase I, leading to the accumulation of high-mannose glycans, which affects glycoprotein processing. | ||||||
Monensin A | 17090-79-8 | sc-362032 sc-362032A | 5 mg 25 mg | $152.00 $515.00 | ||
Alters Golgi ion gradients, affecting glycosylation and the proper processing of glycoproteins. | ||||||