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Rabbit Anti-GH1  antibody (bs-6579R)  
~~~促銷代碼KT202411~~~
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產品編號 bs-6579R
英文名稱 Rabbit Anti-GH1  antibody
中文名稱 生長激素抗體
別    名 SOMA_HUMAN; Somatotropin; Growth hormone (GH; GH-N); Growth hormone 1; Pituitary growth hormone; GHN; GHB5; IGHD2; hGH-N; IGHD1A; IGHD1B;  
Specific References  (2)     |     bs-6579R has been referenced in 2 publications.
[IF=2.445] Xie W et al. Seasonal?expressions?of?growth?hormone?receptor,?insulin-like?growth?factor?1?and?insulin-likegrowth?factor?1?receptor?in the?scented?glands?of the?muskrats?(Ondatra?zibethicus). Gen Comp Endocrinol. 2019 May 20;281:58-66.  IHC-P ;  muskrat.  
[IF=1.399] Jiuxiu Jiet al. The effect of miR‐10b on growth hormone in pituitary cells of Yanbian yellow cattle by somatostatin receptor 2. Anim Sci J . Jan-Dec 2020;91(1):e13420.  WB ;  yellow cattle.  
研究領域 細胞生物  發(fā)育生物學  信號轉導  生長因子和激素  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 (predicted: Human)
產品應用 WB=1:500-2000,IHC-P=1:100-500,IHC-F=1:100-500,IF=1:100-500,ELISA=1:5000-10000
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
理論分子量 21kDa
細胞定位 分泌型蛋白 
性    狀 Liquid
濃    度 1mg/ml
免 疫 原 Recombinant human GH1 protein: full length 
亞    型 IgG
純化方法 affinity purified by Protein A
緩 沖 液 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
保存條件 Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles.
注意事項 This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
PubMed PubMed
產品介紹 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.

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.

Subunit:
Monomer, dimer, trimer, tetramer and pentamer, disulfide-linked or non-covalently associated, in homopolymeric and heteropolymeric combinations. Can also form a complex either with GHBP or with the alpha2-macroglobulin complex.

Subcellular Location:
Secreted.

DISEASE:
Defects in GH1 are a cause of growth hormone deficiency isolated type 1A (IGHD1A); 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); 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) ; also known as pituitary dwarfism VI.
Defects in GH1 are a cause of growth hormone deficiency isolated type 2 (IGHD2). 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.

Similarity:
Belongs to the somatotropin/prolactin family.

SWISS:
P01241

Gene ID:
2688

Database links:

Entrez Gene: 2688 Human

Omim: 139250 Human

SwissProt: P01241 Human

Unigene: 655229 Human



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