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Factor 10 Heavy Chain 抗体 (Alexa Fluor 594)

适用: 人, 小鼠, 大鼠 WB, IF (p) 宿主: 兔 Polyclonal Alexa Fluor 594
产品编号 ABIN2813023
发货至: 中国
  • 抗原
    Factor 10 Heavy Chain
    适用
    人, 小鼠, 大鼠
    宿主
    • 29
    克隆类型
    • 29
    多克隆
    标记
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    Alexa Fluor 594
    应用范围
    • 29
    • 25
    • 13
    • 6
    • 3
    • 3
    Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
    交叉反应
    人, 小鼠, 大鼠
    纯化方法
    Purified by Protein A.
    免疫原
    KLH conjugated synthetic peptide derived from human Activated factor Xa heavy chain
    亚型
    IgG
  • 应用备注
    IF(IHC-P) 1:50-200
    限制
    仅限研究用
  • 状态
    Liquid
    浓度
    1 μg/μL
    缓冲液
    Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
    储存液
    ProClin
    注意事项
    This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
    储存条件
    -20 °C
    储存方法
    Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
    有效期
    12 months
  • 抗原
    Factor 10 Heavy Chain
    别名
    FX antibody, FXA antibody, Cf10 antibody, fX antibody, coagulation factor X antibody, F10 antibody
    背景

    Synonyms: Activated factor Xa heavy chain, Coagulation factor, Coagulation factor X, EC 3.4.21.6, F10 antibody FA10_HUMAN, Factor Xa, FX, FXA, OTTHUMP00000018735, Prothrombinase, Stuart factor, Stuart Prower factor, Stuart-Prower factor, Coagulation factor X, Factor X heavy chain.

    Background: Hemostasis following tissue injury involves the deployment of essential plasma procoagulants (Prothrombin and Factors X, IX, V and VIII), which are involved in a blood coagulation cascade that leads to the formation of insoluble Fibrin clots and the promotion of platelet aggregation. Coagulation Factor X (Stuart Prower factor, FX, F10) is a vitamin K-dependent, single chain serine protease that is synthesized in the liver and circulates as an inactive precursor. The mature form of Factor X (Factor X A) is generated by Factor IX A- or Factor VII A-mediated cleavage at the tripeptide sequence, Arg-Lys-Arg, to yield a disulfide linked dimer. Together with the cofactor Factor V A and Ca2+ on the surface of platelets or endothelial cells, Factor X A coordinates as part of the prothrombinase complex, which mediates proteolysis of Prothrombin into active Thrombin. Mutations at the Factor X locus resulting in Factor X deficiencies can contribute to hemorrhagic diathesis.

    基因ID
    2159
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