Somatotropin Polyclonal Antibody

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商品货号： PLA018178

适应性： 人,大鼠,小鼠,

￥600元

规格：

40μL 100μL 200μL

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MSDS

说明书

商品描述

基因名称： GH1
蛋白名称： Somatotropin
Human_gene_id： 2688
Human_gene_link： http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=2688
Human_swiss_prot_no： P01241
Human_swiss_link： http://www.uniprot.org/uniprotkb/P01241/entry
Mouse_swiss_prot_no： P06880
Mouse_swiss_link： http://www.uniprot.org/uniprot/P06880
特异性： Somatotropin Polyclonal Antibody detects endogenous levels of Somatotropin protein.
组成： Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
来源： Polyclonal, Rabbit,IgG
稀释： IHC 1:100 - 1:300. ELISA: 1:20000.. IF 1:50-200
纯化工艺： The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
浓度： 1 mg/ml
储存： -15°C to -25°C/1 year(Do not lower than -25°C)
说明书： 1
Msds： MSDS_Antibody.pdf
其他名称： GH1; Somatotropin; Growth hormone; GH; GH-N; Growth hormone 1; Pituitary growth hormone
分子量： 25kD
信号通路： Cytokine-cytokine receptor interaction;Neuroactive ligand-receptor interaction;Jak_STAT;
功能： alternative products:Additional isoforms seem to exist,disease:Defects in GH1 are a cause of isolated growth hormone deficiency type IB (IGHD IB) [MIM:262400]; also known as pituitary dwarfism I. IGHD IB is an autosomal recessive deficiency of GH which causes short stature.,disease:Defects in GH1 are a cause of isolated growth hormone deficiency type II (IGHD II) [MIM:173100]. IGHD II is an autosomal dominant deficiency of GH which causes short stature.,disease:Defects in GH1 are the cause of Kowarski syndrome [MIM:262650]; also known as pituitary dwarfism VI.,disease:Defects in GH1 may be a cause of short stature [MIM:604271]. Short stature is defined by a subnormal rate of growth.,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.,miscellaneous:Circulating GH shows a great heterogeneity due to alternative splicing, differential post-translational modifications of monomeric forms, oligomerization, optional binding to 2 different GH-binding proteins, and potentially proteolytic processing.,online information:Growth hormone entry,pharmaceutical:Available under the names Nutropin or Protropin (Genentech), Norditropin (Novo Nordisk), Genotropin (Pharmacia Upjohn), Humatrope (Eli Lilly) and Saizen or Serostim (Serono). Used for the treatment of growth hormone deficiency and for Turner's syndrome.,similarity:Belongs to the somatotropin/prolactin family.,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.,
相关产品： YT4366,YM6184,RS0001,RS0002,YM3028,YM3029
细胞定位： Secreted.
组织表达： Pituitary,
科研货号： PLA018178

Somatotropin Polyclonal Antibody

Catalog No PLA018178

Product information

基因名称： GH1
蛋白名称： Somatotropin
Human_gene_id： 2688
Human_gene_link： http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=2688
Human_swiss_prot_no： P01241
Human_swiss_link： http://www.uniprot.org/uniprotkb/P01241/entry
Mouse_swiss_prot_no： P06880
Mouse_swiss_link： http://www.uniprot.org/uniprot/P06880
特异性： Somatotropin Polyclonal Antibody detects endogenous levels of Somatotropin protein.
组成： Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
来源： Polyclonal, Rabbit,IgG
稀释： IHC 1:100 - 1:300. ELISA: 1:20000.. IF 1:50-200
纯化工艺： The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
浓度： 1 mg/ml
储存： -15°C to -25°C/1 year(Do not lower than -25°C)
说明书： 1
Msds： MSDS_Antibody.pdf
其他名称： GH1; Somatotropin; Growth hormone; GH; GH-N; Growth hormone 1; Pituitary growth hormone
分子量： 25kD
信号通路： Cytokine-cytokine receptor interaction;Neuroactive ligand-receptor interaction;Jak_STAT;
功能： alternative products:Additional isoforms seem to exist,disease:Defects in GH1 are a cause of isolated growth hormone deficiency type IB (IGHD IB) [MIM:262400]; also known as pituitary dwarfism I. IGHD IB is an autosomal recessive deficiency of GH which causes short stature.,disease:Defects in GH1 are a cause of isolated growth hormone deficiency type II (IGHD II) [MIM:173100]. IGHD II is an autosomal dominant deficiency of GH which causes short stature.,disease:Defects in GH1 are the cause of Kowarski syndrome [MIM:262650]; also known as pituitary dwarfism VI.,disease:Defects in GH1 may be a cause of short stature [MIM:604271]. Short stature is defined by a subnormal rate of growth.,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.,miscellaneous:Circulating GH shows a great heterogeneity due to alternative splicing, differential post-translational modifications of monomeric forms, oligomerization, optional binding to 2 different GH-binding proteins, and potentially proteolytic processing.,online information:Growth hormone entry,pharmaceutical:Available under the names Nutropin or Protropin (Genentech), Norditropin (Novo Nordisk), Genotropin (Pharmacia Upjohn), Humatrope (Eli Lilly) and Saizen or Serostim (Serono). Used for the treatment of growth hormone deficiency and for Turner's syndrome.,similarity:Belongs to the somatotropin/prolactin family.,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.,
相关产品： YT4366,YM6184,RS0001,RS0002,YM3028,YM3029
细胞定位： Secreted.
组织表达： Pituitary,
科研货号： PLA018178

Hunan UPT Biotechnology Co.,Ltd

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