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Von Willebrand Factor/vWF Protein, Human, Recombinant (aa 1277-1453, His) is expressed in E. coli. The accession number is P04275.
Pack Size | Price | Availability | Quantity |
---|---|---|---|
100 μg | $687 | Backorder | |
1 mg | $4,530 | Backorder |
Biological Activity | Activity testing is in progress. It is theoretically active, but we cannot guarantee it. If you require protein activity, we recommend choosing the eukaryotic expression version first. |
Description | Von Willebrand Factor/vWF Protein, Human, Recombinant (aa 1277-1453, His) is expressed in E. coli. The accession number is P04275. |
Species | Human |
Expression System | E. coli |
Tag | C-His |
Accession Number | P04275 |
Synonyms | VWF,VWD,F8VWF |
Construction | A DNA sequence encoding the Human vWF (P04275) (Asp1277-Ile1453) was expressed with a polyhistidine tag at the C-terminus. |
Protein Purity | ≥ 90% as determined by SDS-PAGE. |
Molecular Weight | 21.27 kDa (predicted) |
Endotoxin | < 1.0 EU per μg of the protein as determined by the LAL method |
Formulation | Lyophilized from sterile 50 mM Tris, 150 mM NaCl 100 mM Arg, 0.03% skl pH 8.0. Please contact us for any concerns or special requirements. Normally 5 % - 8 % trehalose, mannitol and 0.01% Tween 80 are added as protectants before lyophilization. Please refer to the specific buffer information in the hardcopy of datasheet or the lot-specific COA. |
Reconstitution | Please refer to the lot-specific COA. |
Stability & Storage | It is recommended to store recombinant proteins at -20°C to -80°C for future use. Lyophilized powders can be stably stored for over 12 months, while liquid products can be stored for 6-12 months at -80°C. For reconstituted protein solutions, the solution can be stored at -20°C to -80°C for at least 3 months. Please avoid multiple freeze-thaw cycles and store products in aliquots. |
Shipping | In general, Lyophilized powders are shipping with blue ice. |
Research Background | Von Willebrand Factor (VWF) is a multimeric glycoprotein involved in hemostasis in blood, binds receptors on the surface of platelets and in connective tissue, thereby mediating the adhesion of platelets to sites of vascular injury. From studies it appears that VWF protein uncoils under these circumstances, decelerating passing platelets. VWF protein is deficient or defective in von Willebrand disease (VWD) and is involved in a large number of other diseases, including thrombosis, thrombotic thrombocytopenic purpura, Stroke, Heyde's syndrome, possibly hemolytic-uremic syndrome and so on. |
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