Anti-Human VWF Polyclonal Antibody

VWF多克隆抗体

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.
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基本信息

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货号 PA12853
规格 100μl
宿主 Rabbit
免疫原 Recombinant protein of human VWF
特异性 Plasma.
亚型 IgG
反应性 Human
克隆
Uniprot P04275
浓度 0.4 mg/mL
推荐稀释度 IHC 1:25-1:100
配方
应用范围 IHC,ELISA
别名 Coagulation factor VIII,Coagulation factor VIII VWF,F8VWF,Factor VIII related antigen,von Willebrand antigen 2,von Willebrand antigen II,Von Willebrand disease,VWD,vWF,VWF
保存条件 冻干产品: 2 - 8°C保存5年; 液体: -20°C保存2年.
注意 仅用于科学研究, 不能用于疾病诊断.

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