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VWF


Official Full Name
von Willebrand factor
Organism
Homo sapiens
Gene ID
7450
Background
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]
Synonyms
VWD; F8VWF

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LV29722L human VWF (NM_000552) lentivirus particles Inquiry
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SHH445512 shRNA set against Human VWF (NM_000552.3) Inquiry
SHH445516 shRNA set against Mouse VWF (NM_011708.4) Inquiry
SHW014239 shRNA set against Danio rerio VWF (NM_001281989) Inquiry
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MiUTR1H-11180 VWF miRNA 3'UTR clone Inquiry
CDCB175714 Danio rerio VWF ORF Clone (NM_001281989) Inquiry
CDCB180979 Rabbit VWF ORF clone (XM_008259716.1) Inquiry
CDCH100488 human VWF ORF clone (NM_000552.3) Inquiry
CDCR251186 Mouse Vwf ORF Clone(NM_011708.4) Inquiry
CDCS405738 Human VWF ORF Clone (BC022258) Inquiry
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