anti-Factor IX antibody

Key features and details

  • 产品描述: Rabbit Polyclonal antibody recognizes Factor IX
  • 反应物种: Hu
  • 应用: WB
  • 宿主: Rabbit
  • 克隆: Polyclonal
  • 同位型: IgG
  • 靶点名称: Factor IX
  • 抗原物种: Human
  • 抗原: Synthetic peptide of Human Factor IX.
  • Brand:
CAT.NO. : ARG41467
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Product Details
概述
产品描述Rabbit Polyclonal antibody recognizes Factor IX
反应物种Hu
应用WB
宿主Rabbit
克隆Polyclonal
同位型IgG
靶点名称Factor IX
抗原物种Human
抗原Synthetic peptide of Human Factor IX.
偶联标记Un-conjugated
別名Coagulation factor IX; HEMB; FIX; PTC; Plasma thromboplastin component; F9 p22; THPH8; EC 3.4.21.22; P19; Christmas factor
应用说明
应用建议
应用推荐稀释比
WB1:500 - 1:2000
应用说明* The dilutions indicate recommended starting dilutions and the optimal dilutions or concentrations should be determined by the scientist.
阳性对照Human plasma
实际分子量~ 63 kDa
属性
形式Liquid
纯化Affinity purified.
缓冲液PBS (pH 7.4), 150 mM NaCl, 0.02% Sodium azide and 50% Glycerol.
抗菌剂0.02% Sodium azide
稳定剂50% Glycerol
存放说明For continuous use, store undiluted antibody at 2-8°C for up to a week. For long-term storage, aliquot and store at -20°C. Storage in frost free freezers is not recommended. Avoid repeated freeze/thaw cycles. Suggest spin the vial prior to opening. The antibody solution should be gently mixed before use.
注意事项For laboratory research only, not for drug, diagnostic or other use.
生物信息
数据库连接

GeneID: 2158 Human F9

Swiss-port # P00740 Human Coagulation factor IX

基因名称F9
全名coagulation factor IX
背景介绍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. Alternative splicing results in multiple transcript variants encoding different isoforms that may undergo similar proteolytic processing. [provided by RefSeq, Sep 2015]
生物功能Factor IX is a vitamin K-dependent plasma protein that participates in the intrinsic pathway of blood coagulation by converting factor X to its active form in the presence of Ca(2+) ions, phospholipids, and factor VIIIa. [UniProt]
细胞定位Secreted. [UniProt]
预测分子量52 kDa
翻译后修饰Activated by factor XIa, which excises the activation peptide (PubMed:9169594, PubMed:1730085). The propeptide can also be removed by snake venom protease (PubMed:20004170, PubMed:20080729).

The iron and 2-oxoglutarate dependent 3-hydroxylation of aspartate and asparagine is (R) stereospecific within EGF domains.

Predominantly O-glucosylated at Ser-99 by POGLUT1 in vitro. Xylosylation at this site is minor. [UniProt]
检测图片 (1)
  • ARG41467 anti-Factor IX antibody WB image

    Western blot: Human plasma lysate stained with ARG41467 anti-Factor IX antibody.

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