VWF Polyclonal Antibody

Product Specifications

Background

Von Willebrand factor (VWF) Homo sapiens 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 ID

7450

Swiss Prot

P04275

Cross Reactivity

Human; Rat; Mouse

Clonality

Polyclonal

Source

Rabbit

Applications

IHC-p; IF (paraffin section)

Dilution

IHC-p 1:50-300

Buffer

Liquid in PBS containing 50% glycerol, and 0.02% sodium azide.

Molecular Weight

309

Storage Conditions

-20°C/1 year

Protein Weight

309