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Anti-Coagulation factor X/F10 Antibody (6U812)

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产品编号 TMAY-01598

Anti-Coagulation factor X/F10 Antibody (6U812) 是一种 Mouse 抗体,靶向 Coagulation factor X/F10。Anti-Coagulation factor X/F10 Antibody (6U812) 可用于 ELISA(Cap)。

Anti-Coagulation factor X/F10 Antibody (6U812)

Anti-Coagulation factor X/F10 Antibody (6U812)

Rating icon 还可以
产品编号 TMAY-01598

Anti-Coagulation factor X/F10 Antibody (6U812) 是一种 Mouse 抗体,靶向 Coagulation factor X/F10。Anti-Coagulation factor X/F10 Antibody (6U812) 可用于 ELISA(Cap)。

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产品介绍

生物活性
产品描述
Anti-Coagulation factor X/F10 Antibody (6U812) is a Mouse antibody targeting Coagulation factor X/F10. Anti-Coagulation factor X/F10 Antibody (6U812) can be used in ELISA(Cap).
Ig Type
Monoclonal Mouse IgG1
克隆号
6U812
交叉反应
Human
应用
ELISA(Cap)
抗体种类
Monoclonal
宿主来源Mouse
构建方式This antibody was produced from a hybridoma resulting from the fusion of a mouse myeloma with B cells obtained from a mouse immunized with purified, recombinant Human Coagulation Factor X/F10 (rh Coagulation Factor X/F10; TMPY-01101; NP_000495.1; Met1-Lys488). The IgG fraction of the cell culture supernatant was purified by Protein A affinity chromatography.
纯化方式Protein A
性状Liquid
缓冲液0.2 μm filtered solution in PBS
研究背景Coagulation factor X, also known as FX, F10, Eponym Stuart-Prower factor, and thrombokinase, is an enzyme of the coagulation cascade. It is one of the vitamin K-dependent serine proteases, and plays a crucial role in the coagulation cascade and blood clotting, as the first enzyme in the common pathway of thrombus formation. Factor X deficiency is one of the rarest of the inherited coagulation disorders. FX deficiency among the most severe of the rare coagulation defects, typically including hemarthroses, hematomas, and umbilical cord, gastrointestinal, and central nervous system bleeding. Factor X is synthesized in the liver as a mature heterodimer formed from a single-chain precursor, and vitamin K is essential for its synthesis. Factor X is activated into factor Xa (FXa) by both factor IX (with its cofactor, factor VIII in a complex known as intrinsic Xase) and factor VII (with its cofactor, tissue factor in a complex known as extrinsic Xase) through cleaving the activation propeptide. As the first member of the final common pathway or thrombin pathway, FXa converts prothrombin to thrombin in the presence of factor Va, Ca2+, and phospholipid during blood clotting and cleaves prothrombin in two places (an arg-thr and then an arg-ile bond). This process is optimized when factor Xa is complexed with activated cofactor V in the prothrombinase complex. Inborn deficiency of factor X is very uncommon, and may present with epistaxis (nose bleeds), hemarthrosis (bleeding into joints) and gastrointestinal blood loss. Apart from congenital deficiency, low factor X levels may occur occasionally in a number of disease states. Furthermore, factor X deficiency may be seen in amyloidosis, where factor X is adsorbed to the amyloid fibrils in the vasculature.
偶联与修饰
偶联
Unconjugated
抗原信息
免疫原
Recombinant Human Coagulation Factor X/F10 Protein (TMPY-01101)
抗原种属
Human
研究领域
Serine Proteases and Regulators
存储&运输
储存方式Store at 2°C-8°C for 1 month. Store at -20°C or -80°C for 12 months. Avoid repeated freeze-thaw cycles. Preservative-Free.
运输方式Shipping with blue ice.

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