本公司产品仅供体外研究使用,不用于临床诊断

Factor IX Polyclonal Antibody

规格: / 20μL / 60μL / 120μL / 200μL
价格: / ¥420 / ¥1010 / ¥1640 / ¥2365

货号:E-AB-14396

宿主: Rabbit

反应性: H,M,R

应用: WB

  • 详情
  • Overview

    Synonyms Christmas Disease,Christmas factor,Coagulant factor IX,Coagulation factor 9,Coagulation factor IX,Coagulation factor IXa heavy chain,F9,FA9,Factor 9,Factor IX Deficiency,FactorIX,FIX,Haemophilia B,HEMB,MGC129641,MGC129642,P19,Plasma Thromboplastic Component,Plasma thromboplastin component,PTC,F9抗体
    Swissprot P00740
    Source Rabbit
    Reactivity Human,Mouse,Rat
    Immunogen Recombinant protein of human F9
    Application WB(Detection kit: E-IR-R304)
    Recommended dilution WB,,1:500-1:2000;
    Concentration 0.2 mg/mL
    Clonality Polyclonal

    Properties

    Cellular localization Secreted.
    Tissue specificity Synthesized primarily in the liver and secreted in plasma.
    Isotype IgG
    Purification Affinity purification
    Conjugation Unconjugated
    Storage instructions Store at -20℃. Avoid freeze / thaw cycles.
    Storage buffer PBS with 0.05% sodium azide, 50% glycerol, PH7.3
    Background This gene encodes vitamin K-dependent coagulation factor IX that circulates in the blood as an inactive zymogen. This factor is converted to an active form by factor XIa, which excises the activation peptide and thus generates a heavy chain and a light chain held together by one or more disulfide bonds. The role of this activated factor IX in the blood coagulation cascade is to activate factor X to its active form through interactions with Ca+2 ions, membrane phospholipids, and factor VIII. Alterations of this gene, including point mutations, insertions and deletions, cause factor IX deficiency, which is a recessive X-linked disorder, also called hemophilia B or Christmas disease.
    如有任何问题,请拨打电话 027-87879180 或填写 在线留言 我们会第一时间联系您。
    ×
    var _hmt = _hmt || []; MIP.watch('count', function () { console.log("sdsfs"); _hmt.push(['_trackEvent', 'consult_mip', 'click', 'detail page']); })