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Protein structure
VWF
Von Willebrand factorF8VWF
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]
Top validated antibodies |
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| Invitrogen Antibodies |  MA5-14029 |
28 references | Monoclonal |
WB
ICC
IHC
FC
OA
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| Proteintech Group | 11778-1-AP |
64 references | Polyclonal |
WB
EL
IP
IHC
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| Novus Biologicals | NBP2-53314-100ug |
Monoclonal |
WB
ICC
IP
IHC
FC
PA
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| GeneTex | GTX74843 |
1 references | Monoclonal |
WB
EL
ICC
IHC
RA
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| NSJ Bioreagents | V3233 |
20 references | Monoclonal |
ICC
IHC
FC
OA
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