Vitronectin (Vitronectin V10 Subunit, Vitronectin V65 Subunit, VN, VNT, VTN, Complement S Protein, Epibolin, S Protein, S-Protein, Serum Spreading Factor, Somatomedin B, Somatomedin-B, V75)
Catalog No : USB-V2200-05
555.19€
0.00€
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| Product name | Vitronectin (Vitronectin V10 Subunit, Vitronectin V65 Subunit, VN, VNT, VTN, Complement S Protein, Epibolin, S Protein, S-Protein, Serum Spreading Factor, Somatomedin B, Somatomedin-B, V75) | ||
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| Catalog No | USB-V2200-05 | ||
| Supplier’s Catalog No | V2200-05 | ||
| Supplier | US Biologicals | ||
| Source antigen | Human plasma | ||
| Reactivity | |||
| Cross reactivity | |||
| Applications | |||
| Molecular weight | |||
| Storage | -20°C | ||
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| Other names | |||
| Grade | Affinity Purified | ||
| Purity | ≥95% based on Coomassie brilliant blue stain of 10% SDS-PAGE. Human vitronectin was purified by the method of Hayman et al. using an anti-vitronectin monoclonal antibody affinity column. Purified protein sterile filtered (0.2um). | ||
| Form | Purified human vitronectin in 0.15M sodium chloride, 0.005M HEPES, pH 7.4. | ||
| Reactivity life | 12 months | ||
| Note | For reserch purpose only | ||
| Purity | ≥95% based on Coomassie brilliant blue stain of 10% SDS-PAGE. Human vitronectin was purified by the method of Hayman et al. using an anti-vitronectin monoclonal antibody affinity column. Purified protein sterile filtered (0.2um). | ||
| Description | Corning 24-well plates were coated with vitronectin in PBS (0.3 mL/well) at 37°C overnight. After blocking with BSA, TIG-3 cells (5 x 10e4 cells/1 mL DMEM/well) were added and incubated at 37°C for 90 minutes. Attached cells were counted electronically with a Coulter counter. Under these conditions, the use of a concentration of 3 mg vitronectin per milliliter resulted in the attachment of > 40% of the cells. Storage and Stability: May be stored at 4°C for short-term only. Aliquot to avoid repeated freezing and thawing. Store at -20°C. Aliquots are 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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