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- 详细信息
- 技术资料
- 保存条件:
常温,避光
- 克隆性:
单克隆
- 抗体名:
vWF抗体
vWF抗体产品信息免疫原 : CHO cell-derived rhvWF ( Catalog#10973-H08C )
抗体宿主 : Rabbit IgG
缓冲液 : 0.2 μm filtered solution in PBS, 5% trehalose may be added in some batches. Please read the hardcopy of COA or contact our customer service to confirm the formulation.
制备方法 : Produced in rabbits immunized with purified, CHO cell-derived, recombinant human von Willebrand factor (rhvWF; Catalog#10973-H08C; aa 1- 2813; NP_000543.2). Total IgG was purified by Protein A affinity chromatography.
vWF抗体背景综述
Von Willebrand factor (vWF) is a blood glycoprotein which is involved in a large number of diseases, including thrombotic thrombocytopenic purpura, Heyde's syndrome, and possibly hemolytic-uremic syndrome. Its primary function is binding to other proteins, particularly Factor VIII and it is important in platelet adhesion to wound sites. vWF appears to play a major role in blood coagulation. Its deficiency or dysfunction leads to a bleeding tendency, which is most apparent in tissues having high blood flow shear in narrow vessels. It appears that vWF uncoils under these circumstances, decelerating passing platelets. Hereditary or acquired defects of vWF lead to von Willebrand disease (vWD), a bleeding diathesis of the skin and mucous membranes, causing menorrhagia, and gastrointestinal bleeding.
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xy-13799R C19orf8019号染色体开放阅读框80抗体
xy-5808R CDO1半胱氨酸双加氧酶1抗体
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xy-1053R CCP瓜氨酸环肽抗体
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xy-6727R CAMK4钙/钙调蛋白依赖性蛋白激酶4抗体
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xy-6804R CEAM3癌胚抗原相关细胞粘附分子3抗体
抗体宿主 : Rabbit IgG
缓冲液 : 0.2 μm filtered solution in PBS, 5% trehalose may be added in some batches. Please read the hardcopy of COA or contact our customer service to confirm the formulation.
制备方法 : Produced in rabbits immunized with purified, CHO cell-derived, recombinant human von Willebrand factor (rhvWF; Catalog#10973-H08C; aa 1- 2813; NP_000543.2). Total IgG was purified by Protein A affinity chromatography.
vWF抗体背景综述
Von Willebrand factor (vWF) is a blood glycoprotein which is involved in a large number of diseases, including thrombotic thrombocytopenic purpura, Heyde's syndrome, and possibly hemolytic-uremic syndrome. Its primary function is binding to other proteins, particularly Factor VIII and it is important in platelet adhesion to wound sites. vWF appears to play a major role in blood coagulation. Its deficiency or dysfunction leads to a bleeding tendency, which is most apparent in tissues having high blood flow shear in narrow vessels. It appears that vWF uncoils under these circumstances, decelerating passing platelets. Hereditary or acquired defects of vWF lead to von Willebrand disease (vWD), a bleeding diathesis of the skin and mucous membranes, causing menorrhagia, and gastrointestinal bleeding.
vWF抗体相关产品如下:xy-6516R CA8碳酸酐酶相关蛋白8抗体
xy-6517R CACNB1钙通道电压依赖性β1蛋白抗体
xy-6526R CD39L4原癌基因CD39样蛋白4抗体
xy-5881R COL20A1胶原样蛋白抗体
xy-5959R CASC5肿瘤易感性候选基因5抗体
xy-6253R CAMKK2钙调蛋白激酶激酶β抗体
xy-5930R Centaurin gamma 1中心体肌动蛋白γ1/增强型PI3K蛋白抗体
xy-5963R CDCA7L细胞分裂周期相关蛋白JPO2抗体
xy-5802R Caspase 2半胱胺酸蛋白酶-2抗体
xy-15278R C7orf637号染色体开放阅读框63抗体
xy-6239R CD2BP3CD2结合蛋白3抗体
xy-5882R CTHRC1胶原三股螺旋重复蛋白1抗体
xy-15115R c20orf7220号染色体开放阅读框72抗体
xy-6549R C2orf62号染色体开放阅读框6抗体
xy-5880R CDCP1CD318抗体
xy-6595R CENPB着丝粒蛋白B抗体
xy-9791R C1ORF1111号染色体开放阅读框111抗体
xy-13799R C19orf8019号染色体开放阅读框80抗体
xy-5808R CDO1半胱氨酸双加氧酶1抗体
xy-2924R Collagen XI alpha 2胶原蛋白11A2抗体
xy-6698R Cullin 4BCUL4B蛋白抗体
xy-9797R C1orf1031号染色体开放阅读框103抗体
xy-5803R API2凋亡抑制因子2抗体
xy-9906R CRHBP促肾上腺皮质激素释放激素结合蛋白抗体
xy-9827R C3orf233号染色体开放阅读框23抗体
xy-1053R CCP瓜氨酸环肽抗体
xy-7051R DENTT细胞分裂核仁蛋白1抗体
xy-6727R CAMK4钙/钙调蛋白依赖性蛋白激酶4抗体
xy-6728R phospho-CAMK4(Thr196 + Thr200)磷酸化钙/钙调蛋白依赖性蛋白激酶4抗体
xy-7501R CO4A2胶原蛋白4a2亚基抗体
xy-4682R CD161cCD161c抗体
xy-15086R C1r补体C1r链多肽抗体
xy-7050R CMG1毛细管形态发生蛋白1抗体
xy-2961R Calsequestrin肌钙集蛋白/收钙素抗体
xy-6802R CAB39L钙结合蛋白样39抗体
xy-6804R CEAM3癌胚抗原相关细胞粘附分子3抗体
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vWF抗体
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