This gene encodes a glycoprotein involved in hemostasis. The encoded preproprotein is proteolytically processed following assembly into large multimeric complexes. These complexes function in the adhesion of platelets to sites of vascular injury and the transport of various proteins in the blood. Mutations in this gene result in von Willebrand disease, an inherited bleeding disorder. An unprocessed pseudogene has been found on chromosome 22. [provided by RefSeq, Oct 2015]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| VWF-20-RE | 20 (40 μL) | 200 μL |  |
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| VWF-20-OR | 20 (40 μL) | 200 μL |  |
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| VWF-20-GO | 20 (40 μL) | 200 μL |  |
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| VWF-20-GR | 20 (40 μL) | 200 μL |  |
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| VWF-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes a glycoprotein involved in hemostasis. The encoded preproprotein is proteolytically processed following assembly into large multimeric complexes. These complexes function in the adhesion of platelets to sites of vascular injury and the transport of various proteins in the blood. Mutations in this gene result in von Willebrand disease, an inherited bleeding disorder. An unprocessed pseudogene has been found on chromosome 22. [provided by RefSeq, Oct 2015]
Gene Symbol : VWF
Gene Name : Von Willebrand factor
Chromosome : CHR 12: 612,467,4-594,887,3
Locus : 12p13.31
Alt. Genes : OPTN
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