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Rabbit Polyclonal Anti-GH antibody (STJ98734)
Supplier: St John’s Laboratory Ltd.
Recommended applications: IHC-P, ELISA
Recommended dilution: IHC-P 1:50-300; ELISA 1:5000-20000
Recommended protocols: check protocols
Click or hover above images to see image description for Anti-GH antibody.
Check alternative names for the antibodyExpand
|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|Anti-Growth Hormone antibody [EPR11047(B)] (ab155276)
SCBT cat No: sc-27091|sc-515021|sc-166696|sc-374266|sc-57158|sc-51602|sc-51910|sc-10364|sc-73289|
|Catalogue No.|| |
Anti-GH antibody detects endogenous GH.
Synthetic peptide from human protein at AA range: 180-217.
|Recommended dilution|| |
IHC-P 1:50-300; ELISA 1:5000-20000
Anti-GH antibody was tube-contained in PBS, pH 7.4, containing 0.02% sodium azide as Preservative and 50% Glycerol.
Anti-GH antibody was affinity-purified from rabbit serum by affinity-chromatography using specific immunogen.
-20 Celsius degree. Avoid repeated freeze/thaw cycles.
|Alternative antibody names|| |
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
|Database links|| |
|Protein function|| |
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.
|Involvement in disease|| |
Growth hormone deficiency, isolated, 1A (IGHD1A) [MIM:262400]: An autosomal recessive, severe deficiency of growth hormone leading to dwarfism. Patients often develop antibodies to administered growth hormone. . Note=The disease is caused by mutations affecting the gene represented in this entry.; Growth hormone deficiency, isolated, 1B (IGHD1B) [MIM:612781]: An autosomal recessive deficiency of growth hormone leading to short stature. Patients have low but detectable levels of growth hormone, significantly retarded bone age, and a positive response and immunologic tolerance to growth hormone therapy. . Note=The disease is caused by mutations affecting the gene represented in this entry.; Kowarski syndrome (KWKS) [MIM:262650]: A syndrome clinically characterized by short stature associated with bioinactive growth hormone, normal or slightly increased growth hormone secretion, pathologically low insulin-like growth factor 1 levels, and normal catch-up growth on growth hormone replacement therapy. . Note=The disease is caused by mutations affecting the gene represented in this entry.; Growth hormone deficiency, isolated, 2 (IGHD2) [MIM:173100]: An autosomal dominant deficiency of growth hormone leading to short stature. Clinical severity is variable. Patients have a positive response and immunologic tolerance to growth hormone therapy. . Note=The disease is caused by mutations affecting the gene represented in this entry.
|Protein sequence and domain|| |
Belongs to the somatotropin/prolactin family.
|Protein cellular localization|| |
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St John’s Laboratory Ltd.
|Product type|| |
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