Anti-Prothrombin抗体(Biotin) (ab79747)

概述

  • 产品名称Anti-Prothrombin抗体(Biotin)
    参阅全部 Prothrombin 一抗
  • 描述
    山羊多克隆抗体to Prothrombin (Biotin)
  • 偶联物Biotin
  • 经测试应用适用于: WB, RIAmore details
  • 种属反应性
    与反应: Mouse
  • 免疫原

    Mouse prothrombin purified from mouse plasma

性能

  • 形式Liquid
  • 存放说明Shipped at 4°C. Store at +4°C short term (1-2 weeks). Store at -20°C or -80°C. Avoid freeze / thaw cycle.
  • 存储溶液Preservative: 0.01% Thimerosal (merthiolate)
    Constituents: 50% Glycerol, PBS, pH 7.5
  • Concentration information loading...
  • 纯度Protein G purified
  • 克隆多克隆
  • 同种型IgG
  • 研究领域

应用

Our Abpromise guarantee covers the use of ab79747 in the following tested applications.

The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.

应用 Ab评论 说明
WB
RIA
  • 应用说明RIA: Use at a concentration of 5 µg/ml.
    EIA: Use at a concentration of 5 µg/ml.
    WB: Use at a concentration of 20 µg/ml. Predicted molecular weight: 70 kDa.


    Not yet tested in other applications.
    Optimal dilutions/concentrations should be determined by the end user.
  • 靶标

    • 功能Thrombin, which cleaves bonds after Arg and Lys, converts fibrinogen to fibrin and activates factors V, VII, VIII, XIII, and, in complex with thrombomodulin, protein C. Functions in blood homeostasis, inflammation and wound healing.
    • 组织特异性Expressed by the liver and secreted in plasma.
    • 疾病相关Defects in F2 are the cause of factor II deficiency (FA2D) [MIM:613679]. It is a very rare blood coagulation disorder characterized by mucocutaneous bleeding symptoms. The severity of the bleeding manifestations correlates with blood factor II levels.
      Genetic variations in F2 may be a cause of susceptibility to ischemic stroke (ISCHSTR) [MIM:601367]; also known as cerebrovascular accident or cerebral infarction. A stroke is an acute neurologic event leading to death of neural tissue of the brain and resulting in loss of motor, sensory and/or cognitive function. Ischemic strokes, resulting from vascular occlusion, is considered to be a highly complex disease consisting of a group of heterogeneous disorders with multiple genetic and environmental risk factors.
      Defects in F2 are a cause of susceptibility to thrombosis (THR) [MIM:188050]. It is a multifactorial disorder of hemostasis characterized by abnormal platelet aggregation in response to various agents and recurrent thrombi formation. Note=A common genetic variation in the 3-prime untranslated region of the prothrombin gene is associated with elevated plasma prothrombin levels and an increased risk of venous thrombosis.
    • 序列相似性Belongs to the peptidase S1 family.
      Contains 1 Gla (gamma-carboxy-glutamate) domain.
      Contains 2 kringle domains.
      Contains 1 peptidase S1 domain.
    • 翻译后修饰The gamma-carboxyglutamyl residues, which bind calcium ions, result from the carboxylation of glutamyl residues by a microsomal enzyme, the vitamin K-dependent carboxylase. The modified residues are necessary for the calcium-dependent interaction with a negatively charged phospholipid surface, which is essential for the conversion of prothrombin to thrombin.
    • 细胞定位Secreted > extracellular space.
    • Information by UniProt
    • 数据库链接
    • 形式Cleaved into the following 4 chains: 1. Activation peptide fragment 1 2. Activation peptide fragment 2 3. Thrombin light chain 4. Thrombin heavy chain
    • 别名
      • coagulation factor II (thrombin) antibody
      • Coagulation factor II antibody
      • F2 antibody
      • Factor II antibody
      • Prepro coagulation factor II antibody
      • Prothrombin antibody
      • prothrombin B-chain antibody
      • PT antibody
      • RPRGL2 antibody
      • serine protease antibody
      • THPH1 antibody
      • THRB antibody
      • THRB_HUMAN antibody
      • Thrombin heavy chain antibody
      see all

    Anti-Prothrombin antibody (Biotin) (ab79747)参考文献

    ab79747 has not yet been referenced specifically in any publications.

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