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The glycoprotein encoded by this gene functions as both an antihemophilic factor carrier and a platelet-vessel wall mediator in the blood coagulation system. It is crucial to the hemostasis process. Mutations in this gene or deficiencies in this protein result in von Willebrand's disease. An unprocessed pseudogene has been found on chromosome 22. [provided by RefSeq, Jul 2008].

推荐稀释比 IHC:1/50-1/100

Immunohistochemistry analysis of paraffin-embedded Human tonsil within the normal limits using von Willebrand Factor antibbody. High-pressure and temperature Tris-EDTA pH 8.0 was used for antigen retrieval.

-25 ~ -15℃保存，收到货之后有效期1年，避免反复冻融。