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        1. 上海允麥生物科技有限公司
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          當(dāng)前位置:首頁   >>   資料下載   >>   VWF抗原,血管假性血友病因子/血管性血友病因子抗原

          VWF抗原,血管假性血友病因子/血管性血友病因子抗原

          時間:2024-11-14閱讀:19
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          Recombinant human VWF protein   

          Von Willebrand Factor; Coagulation factor VIII; F8VWF; Factor VIII related antigen; von Willebrand antigen 2; Von Willebrand antigen II; Von Willebrand disease; VWD; VWF_HUMAN.   

          濃度:1mg/ ml

          來源:Recombinant Human

          純度:95% SDS-PAGE

          表達(dá)系統(tǒng):Wheat germ

          標(biāo)簽:GST tag N-Terminus

          蛋白長度:Protein fragment

          內(nèi)毒素水平:<1.000 Eu/µg

          純化方法:HPLC

          應(yīng)用:SDS-PAGEWestern blot,ELISA

          Biological activity,immunology research

          保存:-20

          保質(zhì)期:1

          Von Willebrand Factor (VWF) was previously known as Factor VIII related antigen. VWF is synthesized exclusively by endothelial cells and megakaryocytes, and stored in the intracellular granules or constitutively secreted into plasma. This glycoprotein functions as both an antihemophilic factor carrier and a platelet vessel wall mediator in the blood coagulation system. Important in the maintenance of homeostasis, it participates in platelet vessel wall interactions by forming a noncovalent complex with coagulation factor VIII at the site of vascular injury. The Von Willebrand factor has functional binding domains to platelet glycoprotein Ib, glycoprotein IIb/IIIa, collagen and heparin. Mutations in this gene or deficiencies in this protein result in Von Willebrand's disease. VWD is characterized by frequent bleeding (gingival, minor skin quantitative lacerations, menorrhagia, etc.).

           



          產(chǎn)品名稱:Rabbit Anti-VWF protein antibody

          Rabbit Anti-VWF protein 

          別名:Von Willebrand Factor; Coagulation factor VIII; F8VWF; Factor VIII related antigen; von Willebrand antigen 2; Von Willebrand antigen II; Von Willebrand disease; VWD; VWF_HUMAN.              

          來源:Rabbit

          克隆類型:Polyclonal

          濃度:1mg/ml

          亞型:IgG

          反應(yīng):Human,Mouse,Rat (predicted: Rabbit,Pig,Cow,Dog)

          應(yīng)用: WB=1:1000-1:2000,Elisa=1:1000-1:2000,IHC-P=1:100-500

                 IHC-F=1:100-500,ICC/IF=1:100-500,IF=1:100-500  Flow-Cyt=3ug/Test

          理論分子量:309 kDa

          免疫原:KLH conjugated synthetic peptide derived from human VWF protein

          保存:-20
          保質(zhì)期:1

           

           

          產(chǎn)品名稱:Anti-VWF protein antibody

          Mouse Anti-VWF protein

          別名:Von Willebrand Factor; Coagulation factor VIII; F8VWF; Factor VIII related antigen; von Willebrand antigen 2; Von Willebrand antigen II; Von Willebrand disease; VWD; VWF_HUMAN.                

          來源:Mouse

          克隆類型:Monoclonal

          濃度:1mg/ml

          亞型:IgG

          反應(yīng):Human

          應(yīng)用:WB=1:1000-1:2000,Elisa=1:1000-1:2000,IHC-P=1:100-500

                 IHC-F=1:100-500,ICC/IF=1:100-500,IF=1:100-500 Flow-Cyt=3ug/Test

          反應(yīng):  Human

          理論分子量:309 kDa

          免疫原:KLH conjugated synthetic peptide derived from human VWF protein

          保存:-20
          保質(zhì)期:1

          Von Willebrand Factor (VWF) was previously known as Factor VIII related antigen. VWF is synthesized exclusively by endothelial cells and megakaryocytes, and stored in the intracellular granules or constitutively secreted into plasma. This glycoprotein functions as both an antihemophilic factor carrier and a platelet vessel wall mediator in the blood coagulation system. Important in the maintenance of homeostasis, it participates in platelet vessel wall interactions by forming a noncovalent complex with coagulation factor VIII at the site of vascular injury. The Von Willebrand factor has functional binding domains to platelet glycoprotein Ib, glycoprotein IIb/IIIa, collagen and heparin. Mutations in this gene or deficiencies in this protein result in Von Willebrand's disease. VWD is characterized by frequent bleeding (gingival, minor skin quantitative lacerations, menorrhagia, etc.).


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