永利3044(中国集团)有限公司官网

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 WB:1/500-1/1000;IHC:1/50-1/100

Western blot analysis of VWF in Human serum lysates using von Willebrand Factor antibody.

-25 ~ -15℃保存，收到货之后有效期1年，避免反复冻融。