Anti-Growth Hormone抗体[GH-2] (ab9822)


  • 产品名称
    Anti-Growth Hormone抗体[GH-2]
    参阅全部 Growth Hormone 一抗
  • 描述
    小鼠单克隆抗体[GH-2] to Growth Hormone
  • 宿主
  • 经测试应用
    适用于: WB, ELISA, Indirect ELISAmore details
  • 种属反应性
    与反应: Human
  • 免疫原

    Recombinant full length protein corresponding to Human Growth Hormone.
    Database link: P01241

  • 常规说明

    This product was changed from ascites to tissue culture supernatant on 28/11/2017. Lot numbers higher than GR172544-1 and GR172544-3 will be from tissue culture supernatant. Please note that the dilutions may need to be adjusted accordingly.



Our Abpromise guarantee covers the use of ab9822 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 1/1000 - 1/5000.
ELISA Use at an assay dependent dilution.
This antibody can be used in two-site immunoassays for the determination of human growth hormone levels. It recognizes a different epitope than GH-1 (ab9821). We recommend using this antibody (ab9822) as the detection antibody
Indirect ELISA 1/1000 - 1/10000.


  • 功能
    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.
  • 疾病相关
    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.
  • 序列相似性
    Belongs to the somatotropin/prolactin family.
  • 细胞定位
  • Information by UniProt
  • 数据库链接
  • 别名
    • gH antibody
    • GH-N antibody
    • GH1 antibody
    • GHB5 antibody
    • GHN antibody
    • Growth hormone 1 antibody
    • Growth hormone antibody
    • Growth hormone B5 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


  • Western blot of human growth hormone using ab9822 at a concentration of 1 µg/ml.




This product has been referenced in:
  • Fradkin AH  et al. Immunogenicity of aggregates of recombinant human growth hormone in mouse models. J Pharm Sci 98:3247-64 (2009). ELISA ; Mouse . Read more (PubMed: 19569057) »
  • Kunert R  et al. CHO-recombinant human growth hormone as a protease sensitive reporter protein. Appl Microbiol Biotechnol 84:693-9 (2009). Read more (PubMed: 19396439) »

See all 3 Publications for this product


Thank you for your interest in ab9822. Our antibodies are not assigned CAS numbers. This product is not considered a chemical reagent. I hope this information is helpful. Please do not hesitate to contact us if you have any additional questions.

The supplier of Growth Hormone antibody (ab9822)has informed me that the binding capacity was not determined. If you have any more questions, please contact us again.