Phaseolus vulgaris (PHA-E)
Catalog No : USB-518629
421.85€
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Product name | Phaseolus vulgaris (PHA-E) | ||
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Catalog No | USB-518629 | ||
Supplier’s Catalog No | 518629 | ||
Supplier | US Biologicals | ||
Source antigen | Kidney bean | ||
Reactivity | |||
Cross reactivity | |||
Applications | |||
Molecular weight | 126 |
Storage | -20°C | ||
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Other names | |||
Grade | Affinity purified | ||
Purity | Affinity purified | ||
Form | Supplied as a lyophilized powder. | ||
Reactivity life | 2 years | ||
Note | For reserch purpose only | ||
Purity | Affinity purified | ||
Description | Affinity purified Phaseolus vulgaris lectin (PHA-E) is tetrameric glycoprotein and responsible for the erythroagglutinating properties of the PHA fraction. It has a carbohydrate specificity towards oligosaccharides and elutes with bovine thyroglobulin or acetic acid. PHA-E will bind to both human erythrocytes and lymphocytes, with a specificity towards blood group A (-SA). There are five times more PHA-E receptors on normal human lymphocytes than there are on erythrocytes. The crystal structure of a ligand-free PHA-E has a typical legume lectin fold characterized by two anti-parallel β-sheets and two short alpha-helices, and contains one GlcNAc residue of the N-linked glycan. Asparagine linked erythrocytes glycopeptide is an inhibitor of PHA-E induced agglutination and mitogenicity, and becomes inactive if treated with β-galactosidase. PHA-E binds di-galactosylated and bisected N-glycan. This lectin is widely used as a biochemical tool for detecting bisecting GlcNAc- and Gal-bearing glycoproteins. Source: Kidney bean Blood Specificity: A (-SA) Sugar Specificity: Complex N-Glycans Inhibitory Carbohydrate: Bovine Thyroglobulin, Acetic Acid Divalent Ions: Ca++, Mn++ Storage and Stability: Lyophilized powder may be stored at -20°C. Stable for 12 months after receipt at -20°C. Reconstitute with sterile buffer or ddH2O. Aliquot to avoid repeated freezing and thawing. Store at -20°C. Reconstituted product is stable for 6 months at -20°C. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Further dilutions can be made in assay buffer. |
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