VWF is important in hemostasis, and genetic defects in the structure and modification of VWF can cause von Willebrand disease (VWD), the most common congenital bleeding disorder in humans.

推荐稀释比 IHC:1/100-1/200

Immunohistochemistry analysis of paraffin-embedded Hemangioma using von Willebrand Factor antibody.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。