Murine Anti-Factor VIII抗体(GMA-8009)
货号：GMA-8009
品牌：Greenmoab
产品特性
Specificity：FVIII A2 domain (residues Glu604-Arg740)1
Immunogen：B-domain deleted recombinant Human Factor VIII
Application：ELISA and Inhibition
| 规格 | 价格 |
|---|---|
| 0.1 mg | ￥咨询 |
| 0.5 mg | ￥咨询 |
产品咨询：info@biopcr.com
产品订购：sales@biopcr.com
技术支持：tech@biopcr.com
服务热线：400-860-6200
详细介绍
产品名称：Murine Anti-Factor VIII抗体(GMA-8009)
别名：Murine Anti-Factor VIII Antibody；Murine Anti-Factor VIII Monoclonal Antibody；Murine Anti-Factor VIII单克隆抗体；Factor VIII抗体；Murine Anti-Factor VIII抗体；小鼠抗凝血因子VIII抗体；Mouse Anti-Factor VIII Antibody；F8抗体
克隆号（Clone）：GMA-8009
背景介绍（Background）：
Factor VIII (FVIII) is a heterodimer consisting of a heavy chain (ranging in mass from 90 to 200 kDa) bound via metal ions to a light chain (80 kDa). In plasma, FVIII circulates in an inactive form bound to von Willebrand factor. Following activation by factor Xa or thrombin, factor VIIIa can function as cofactor for the enzyme factor IXa in the activation of factor X in the presence of phospholipid and Ca2+. Absent or defective FVIII is the cause of the X-linked recessive bleeding disorder hemophilia A. GMA-8009 (also known as 1D4 or 1D4.1B)1 recognizes the A2 domain of FVIII and inhibits FVIII activation by thrombin or factor Xa. It is suitable for immunohistochemistry and FACS2, ELISA and bio-layer interferometry pairing experiments.
种属反应性（Species Reactivity）: Human
来源（Source）： Murine
特异性（Specificity）： FVIII A2 domain (residues Glu604-Arg740)1
免疫原（Immunogen）： B-domain deleted recombinant Human Factor VIII
亚型（Isotype）： IgG2a
应用（Application）：
ELISA： Binds the A2 domain of recombinant human factor VIII in solid-phase ELISA.
Immunoblotting： Not recommended.
Inhibition： Strongly inhibitory in aPTT clotting assay.
储存（Storage）：Aliquot and store at -20℃ for prolonged periods. Avoid freeze-thaw cycles. Alternatively, add 0.02% (w/v) sodium azide and store at 4℃.
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背景介绍（Background）：
Factor VIII (FVIII) is a heterodimer consisting of a heavy chain (ranging in mass from 90 to 200 kDa) bound via metal ions to a light chain (80 kDa). In plasma, FVIII circulates in an inactive form bound to von Willebrand factor. Following activation by factor Xa or thrombin, factor VIIIa can function as cofactor for the enzyme factor IXa in the activation of factor X in the presence of phospholipid and Ca2+. Absent or defective FVIII is the cause of the X-linked recessive bleeding disorder hemophilia A. GMA-8009 (also known as 1D4 or 1D4.1B)1 recognizes the A2 domain of FVIII and inhibits FVIII activation by thrombin or factor Xa. It is suitable for immunohistochemistry and FACS2, ELISA and bio-layer interferometry pairing experiments.
种属反应性（Species Reactivity）: Human
来源（Source）： Murine
特异性（Specificity）： FVIII A2 domain (residues Glu604-Arg740)1
免疫原（Immunogen）： B-domain deleted recombinant Human Factor VIII
亚型（Isotype）： IgG2a
应用（Application）：
ELISA： Binds the A2 domain of recombinant human factor VIII in solid-phase ELISA.
Immunoblotting： Not recommended.
Inhibition： Strongly inhibitory in aPTT clotting assay.
储存（Storage）：Aliquot and store at -20℃ for prolonged periods. Avoid freeze-thaw cycles. Alternatively, add 0.02% (w/v) sodium azide and store at 4℃.
