Galanthus nivalis (Snowdrop bulb) (GNA) (AP)
Catalog No : USB-G1044-10
444.84€
0.00€
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Product name | Galanthus nivalis (Snowdrop bulb) (GNA) (AP) | ||
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Catalog No | USB-G1044-10 | ||
Supplier’s Catalog No | G1044-10 | ||
Supplier | US Biologicals | ||
Source antigen | Galanthus nivalis (snowdrop bulb) | ||
Reactivity | |||
Cross reactivity | |||
Applications | |||
Molecular weight | 263044 |
Storage | 4°C Do Not Freeze | ||
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Other names | |||
Grade | Molecular Biology Grade | ||
Purity | Highly purified. Three bands at 26kD, 30kD and 44kD detected by SDS-PAGE. | ||
Form | Supplied as a liquid in PBS, pH 7.2-7.4, 20% glycerol.. Labeled with alkaline phosphatase (AP). | ||
Reactivity life | 12 months | ||
Note | For reserch purpose only | ||
Purity | Highly purified. Three bands at 26kD, 30kD and 44kD detected by SDS-PAGE. | ||
Description | Galanthus nivalis agglutinin (GNA) is a small molecular weight tetramer consisting of subunits of about 13,000D. This lectin contains little or no carbohydrate. Unlike most mannose-specific lectins, it is not a metalloprotein and does not require Ca++ or Mn++ for binding. Binding seems to be preferentially directed toward structures containing (a-1,3) mannose residues. In contrast to most mannose-binding lectins, GNA will not bind alpha linked glucose. Reports indicate that this lectin binds IgM, but not bind IgG immunoglobulin classes of rat and mouse. The only protein from human serum reported to bind to this lectin is a2-macroglobulin. Isoelectric Point: < pH 4.6 Activity (unconjugated): ≤ 15ug/ml will agglutinate human type O erythrocytes. Carbohydrate Specificity: Mannose Inhibitory Carbohydrate: Mannose a-1,3-mannose Mannose (> 0.2M ) Inhibiting/Eluting Sugar: 100mM-200mM a-methyl mannoside Activity: Less than 15 mg/ml will agglutinate human type O erythrocytes. Storage and Stability: May be stored at 4°C. For long-term storage, aliquot and store at 4°C. Do not freeze. Aliquots are stable for at least 12 months. 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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