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Factor VII 抗体 (Cleaved-Ala61, Light Chain)

The 兔 多克隆 anti-Factor VII antibody (ABIN8120641) specifically detects Factor VII in WB 和 ELISA. The antibody is reactive with 人, 小鼠 和 大鼠 samples.
产品编号 ABIN8120641
发货至: 中国
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Quick Overview for Factor VII 抗体 (Cleaved-Ala61, Light Chain) (ABIN8120641)

抗原

See all Factor VII (F7) 抗体
Factor VII (F7) (Coagulation Factor VII (F7))

适用

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人, 小鼠, 大鼠

宿主

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  • 8
  • 2
  • 1
兔

克隆类型

  • 86
  • 40
多克隆

标记

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This Factor VII antibody is un-conjugated

应用范围

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Western Blotting (WB), ELISA
  • 抗原表位

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    • 1
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    Cleaved-Ala61, Light Chain

    原理

    FA7 (light chain, Cleaved-Ala61) Antibody

    特异性

    This antibody detects endogenous levels of Human FA7 (light chain, Cleaved-Ala61, protein was cleaved amino acid sequence between 60-61 )

    纯化方法

    The antibody was affinity-purified from rabbit serum by affinity-chromatography using specific immunogen.

    免疫原

    Synthesized peptide derived from human FA7 (light chain, Cleaved-Ala61)

    亚型

    IgG
  • 应用备注

    WB 1:1000-2000 ELISA 1:5000-20000

    限制

    仅限研究用
  • 状态

    Liquid

    缓冲液

    Liquid in PBS containing 50 % glycerol, 0.5 % BSA and 0.02 % sodium azide.

    储存液

    Sodium azide

    注意事项

    This product contains Sodium azide: 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/1 year

    有效期

    12 months
  • 抗原

    Factor VII (F7) (Coagulation Factor VII (F7))

    别名

    FA7

    背景

    Synonyms: Coagulation factor VII (EC 3.4.21.21, Proconvertin, Serum prothrombin conversion accelerator, SPCA, Eptacog alfa) [Cleaved into: Factor VII light chain, Factor VII heavy chain]

    Background: catalytic activity:Selective cleavage of Arg-|-Ile bond in factor X to form factor Xa.,disease:Defects in F7 are the cause of factor VII deficiency [MIM:227500]. Factor VII deficiency is a rare hereditary hemorrhagic disease. The clinical picture can be very severe, with the early occurrence of intracerebral hemorrhages or hemarthroses, or, in contrast, moderate with cutaneous-mucosal hemorrhages (epistaxis, menorrhagia) or hemorrhages provoked by a surgical intervention. Numerous subjects are completely asymptomatic despite a very low F7 level.,function:Initiates the extrinsic pathway of blood coagulation. Serine protease that circulates in the blood in a zymogen form. Factor VII is converted to factor VIIa by factor Xa, factor XIIa, factor IXa, or thrombin by minor proteolysis. In the presence of tissue factor and calcium ions, factor VIIa then converts factor X to factor Xa by limited proteolysis. Factor VIIa will also convert factor IX to factor IXa in the presence of tissue factor and calcium.,online information:Factor VII entry,online information:The Singapore human mutation and polymorphism database,pharmaceutical:Available under the names Niastase or Novoseven (Novo Nordisk). Used for the treatment of bleeding episodes in hemophilia A or B patients with antibodies to coagulation factors VIII or IX.,polymorphism:Individuals with the Q allele (Gln-413) seems to have a decreased susceptibility to myocardial infarction.,PTM:The iron and 2-oxoglutarate dependent 3-hydroxylation of aspartate and asparagine is (R) stereospecific within EGF domains.,PTM:The vitamin K-dependent, enzymatic carboxylation of some glutamate residues allows the modified protein to bind calcium.,similarity:Belongs to the peptidase S1 family.,similarity:Contains 1 Gla (gamma-carboxy-glutamate) domain.,similarity:Contains 1 peptidase S1 domain.,similarity:Contains 2 EGF-like domains.,subunit:Heterodimer of a light chain and a heavy chain linked by a disulfide bond.,tissue specificity:Plasma.,

    Gene Name: F7

    Protein Name: FA7 (light chain, Cleaved-Ala61)

    基因ID

    2155

    UniProt

    P08709

    途径

    Response to Growth Hormone Stimulus, Platelet-derived growth Factor Receptor Signaling
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