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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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