Anti-Growth Hormone 抗体 [GH-Px-2] (ab765)

製品の概要

  • 製品名Anti-Growth Hormone antibody [GH-Px-2]
    Growth Hormone 一次抗体 製品一覧
  • 製品の詳細
    Mouse monoclonal [GH-Px-2] to Growth Hormone
  • 特異性Simultaneously binds to human growth hormone and horseradish peroxidase, eliminating the need for a conjugated secondary antibody.
  • アプリケーション適用あり: IHC-P, ICCmore details
  • 種交差性
    交差種: Human

製品の特性

  • 製品の状態Liquid
  • 保存方法Shipped at 4°C. Store at +4°C short term (1-2 weeks). Upon delivery aliquot. Store at -20°C or -80°C. Avoid freeze / thaw cycle.
  • バッファーPreservative: 15mM Sodium Azide
    Constituents: PBS, pH 7.4
  • Concentration information loading...
  • 精製度>95% by SDS-PAGE
  • 特記事項(精製)Purified from ascites using protein A-affinity chromatography.
  • ポリ/モノモノクローナル
  • クローン名GH-Px-2
  • 研究分野

アプリケーション

Our Abpromise guarantee covers the use of ab765 in the following tested applications.

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

アプリケーション Abreviews 特記事項
IHC-P
ICC
  • 追加情報ICC: Use at an assay dependant dilution.
    IHC-P: Use at an assay dependant concentration.

    Not tested in other applications.
    Optimal dilutions/concentrations should be determined by the end user.
  • ターゲット情報

    • 機能Plays an important role in growth control. Its major role in stimulating body growth is to stimulate the liver and other tissues to secrete IGF-1. It stimulates both the differentiation and proliferation of myoblasts. It also stimulates amino acid uptake and protein synthesis in muscle and other tissues.
    • 関連疾患Defects in GH1 are a cause of growth hormone deficiency isolated type 1A (IGHD1A) [MIM:262400]; also known as pituitary dwarfism I. IGHD1A is an autosomal recessive deficiency of GH which causes short stature. IGHD1A patients have an absence of GH with severe dwarfism and often develop anti-GH antibodies when given exogenous GH.
      Defects in GH1 are a cause of growth hormone deficiency isolated type 1B (IGHD1B) [MIM:612781]; also known as dwarfism of Sindh. IGHD1B is an autosomal recessive deficiency of GH which causes short stature. IGHD1B patients have low but detectable levels of GH. Dwarfism is less severe than in IGHD1A and patients usually respond well to exogenous GH.
      Defects in GH1 are the cause of Kowarski syndrome (KWKS) [MIM:262650]; also known as pituitary dwarfism VI.
      Defects in GH1 are a cause of growth hormone deficiency isolated type 2 (IGHD2) [MIM:173100]. IGHD2 is an autosomal dominant deficiency of GH which causes short stature. Clinical severity is variable. Patients have a positive response and immunologic tolerance to growth hormone therapy.
    • 配列類似性Belongs to the somatotropin/prolactin family.
    • 細胞内局在Secreted.
    • Information by UniProt
    • 参照データベース
    • 別名
      • gH antibody
      • GH-N antibody
      • GH1 antibody
      • GHN antibody
      • Growth hormone 1 antibody
      • Growth hormone antibody
      • Growth hormone, normal antibody
      • Growth hormone, pituitary antibody
      • HG1 antibody
      • hGH-N antibody
      • IGHD1B antibody
      • Pituitary growth hormone antibody
      • RNGHGP antibody
      • SOMA_HUMAN antibody
      • Somatotropin antibody
      see all

    Anti-Growth Hormone antibody [GH-Px-2] (ab765) 使用論文

    ab765 has not yet been referenced specifically in any publications.

    Product Wall

    I have enquired with the suppliers of the other Growth hormone antibodies that we carry, and as for ab765 the supplier informed me that no, the binding capacity has not been determined.

    It has not been tested in ELISA but there is no reason that it should not work. Please use the protocol that is listed under the ELISA protocols link on the Abcam website, which we find excellent.

    Ab765 has not been tested in ELISA, therefore we can't guarantee results. We do not do a ready to use ELISA kit featuring this antibody.

    Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"