背景：Von Willebrand Factor （VWF） is a multimeric glycoprotein involved in hemostasis in blood, binds receptors on the surface of platelets and in connective tissue, thereby mediating the adhesion of platelets to sites of vascular injury.
From studies it appears that VWF protein uncoils under these circumstances, decelerating passing platelets.
VWF protein is deficient or defective in von Willebrand disease （VWD） and is involved in a large number of other diseases, including thrombosis, thrombotic thrombocytopenic purpura, Stroke, Heyde's syndrome, possibly hemolytic-uremic syndrome and so on.
仕様
サイズ：1mg
種由来：Human
発現宿主：CHO Stable Cells
純度：＞75 ％ as determined by reducing SDS-PAGE.
エンドトキシン濃度：＜1.0 EU per μg of the protein as determined by the LAL method.
アクセッションNo.：NP_000543.2
アミノ酸配列：Met 1-Lys 2813
遺伝子構造：A DNA sequence encoding the pro form of human von Willebrand factor （NP_000543.2） （Met 1-Lys 2813） was expressed with a C-terminal polyhistidine tag.
別名（遺伝子名）：F8VWF;Von Willebrand Factor;VWD
分子量：308 kDa
組成：Lyophilized from sterile PBS, pH 7.4
保存条件：Generally, lyophilized proteins are stable for up to 12 months when stored at -20 to -80℃. Reconstituted protein solution can be stored at 4-8℃ for 2-7 days. Aliquots of reconstituted samples are stable at ＜ -20℃ for 3 months.
