产品概述
产品性能
免疫原
产品应用
研究背景
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.
研究领域
Cardiovascular
产品概述
| 产品名称(Product Name) | von Willebrand Factor Rabbit Monoclonal Antibody  | 
| 描述(Description) | Rabbit Monoclonal antibody  | 
| 宿主(Host) | Rabbit  | 
| 应用(Application) | WB,IHC-P  | 
| 种属反应性(Reactivity) | Rat  | 
产品性能
| 偶联物(Conjugation) | Unconjugated  | 
| 修饰(Modification) | Unmodified  | 
| 同种型(Isotype) | IgG  | 
| 克隆(Clonality) | Monoclonal Antibody  | 
| 形式(Form) | Liquid  | 
| 存放说明(Storage) | Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles.  | 
| 储存溶液(Buffer) | 50mM Tris-Glycine(pH 7.4), 0.15M NaCl, 40% Glycerol, 0.01% Sodium azide and 0.05% BSA  | 
| 纯化方式(Purification) | Affinity Purification  | 
免疫原
| 基因名(Gene Name) | VWF  | 
| 别名(Alternative Names) | VWF; von Willebrand factor; von Willebrand antigen II; F8VWF  | 
| 基因ID(Gene ID) | 7450  | 
| 蛋白ID(SwissProt ID) | P04275  | 
产品应用
| 稀释比(Dilution Ratio) | WB: 1:500-1:1000 IHC: 1:50-1:100  | 
| 蛋白分子量(Molecular Weight) | Calculated MW: 309 kDa; Observed MW: 309 kDa  | 
研究背景
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.
研究领域
Cardiovascular