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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

              發(fā)布時(shí)間:2024/11/14點(diǎn)擊次數(shù):35

              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 blotELISA

              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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              精品乱子伦一区二区三区_亚洲精品乱码久久久久久按摩_亚洲久久久久久久_日韩av亚洲欧美一区二区三区_来一水AV@lysav
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