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Factor VII 抗体 (AA 366-466)

The 小鼠 单克隆 anti-Factor VII antibody (Clone F7-3515) (ABIN7874356) specifically detects Factor VII in ELISA 和 IHC (p). The antibody is reactive with 人 samples.
产品编号 ABIN7874356
发货至: 中国
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Quick Overview for Factor VII 抗体 (AA 366-466) (ABIN7874356)

抗原

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

适用

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宿主

  • 62
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小鼠

克隆类型

  • 75
  • 39
单克隆

标记

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This Factor VII antibody is un-conjugated

应用范围

  • 66
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ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

质量等级

Carrier-free

克隆位点

F7-3515
  • 抗原表位

    • 27
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    AA 366-466

    原理

    F7 Antibody / Coagulation Factor VII (azide and preservative free)

    纯化方法

    Protein A/G affinity

    免疫原

    A recombinant partial protein sequence (within amino acids 366-466) from the human protein was used as the immunogen for the F7 antibody.

    亚型

    IgG2, kappa
  • 应用备注

    Optimal dilution of the F7 antibody should be determined by the researcher.

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    1 mg/mL

    缓冲液

    1 mg/mL in 1X PBS, BSA free, sodium azide free

    储存液

    Azide free

    储存条件

    -20 °C

    储存方法

    Aliquot the F7 antibody and store frozen at -20oC or colder. Avoid repeated freeze-thaw cycles.
  • 抗原

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

    别名

    F7

    背景

    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 VII (serum prothrombin conversion accelerator, proconvertin, F7, Factor VII) is a 406 amino acid, vitamin K-dependent, single chain serine protease that is synthesized in the liver and circulates as an inactive precursor. Factor IX A, Factor X A, Factor XII A or Thrombin-mediated proteolytic cleavage of Factor VII at Arg 152-Ile 153 generates Factor VII A, an active serine protease composed of a catalytic heavy chain disulfide linked to a light chain, containing two EGF-like domains. Mutations at the F7 locus that lead to Factor VII deficiencies are generally asymptomatic or phenotypically uncharacterized, with hemorrhagic diathesis occurring at extremely low levels.

    UniProt

    P08709

    途径

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