GSX1/GSH1 抗体 (AA 165-264) (Cy3)
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- 抗原 See all GSX1/GSH1 (GSX1) 抗体
- GSX1/GSH1 (GSX1) (GS Homeobox 1 (GSX1))
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抗原表位
- AA 165-264
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适用
- 小鼠
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宿主
- 兔
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克隆类型
- 多克隆
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标记
- This GSX1/GSH1 antibody is conjugated to Cy3
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应用范围
- Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunofluorescence (Cultured Cells) (IF (cc))
- 交叉反应
- 小鼠
- 预测反应
- Human,Rat,Dog,Sheep,Pig
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human Gsh1
- 亚型
- IgG
- Top Product
- Discover our top product GSX1 Primary Antibody
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- 应用备注
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IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200 - 限制
- 仅限研究用
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- 状态
- Liquid
- 浓度
- 1 μg/μL
- 缓冲液
- Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
- 储存液
- ProClin
- 注意事项
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
- 储存条件
- -20 °C
- 储存方法
- Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
- 有效期
- 12 months
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- 抗原
- GSX1/GSH1 (GSX1) (GS Homeobox 1 (GSX1))
- 别名
- Gsh1 (GSX1 产品)
- 别名
- gsh1 antibody, im:7138106 antibody, zgc:110817 antibody, GSH1 antibody, gsh-1 antibody, Gsh-1 antibody, Gsh1 antibody, GS homeobox 1 antibody, gsx1 antibody, GSX1 antibody, Gsx1 antibody
- 背景
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Synonyms: GS homeo box protein 1, GS homeobox 1, GSH1, GSX1, GSX1_HUMAN, Homeobox protein GSH-1 , Homeobox protein Gsh1.
Background: Growth hormone-releasing hormone (GHRH) stimulates secretion and synthesis of growth hormone (GH), causes somatotroph proliferation and may have direct actions in fetal/placental development, reproduction and immune function. It exerts its action through high-affinity GHRH receptors present in the anterior pituitary. GSH-1 (GS homeobox 1) is a 264 amino acid hypothalamic nuclear protein that functions as a transcription factor responsible for maintaining GHRH expression as well as playing an important role in pituitary development. Coexpression of CBP leads to significantly enhanced GSH-1-induced GHRH expression, which suggest that CBP may function as a co-activator. Knockdown of GSH-1 mRNA in mice causes a dwarf phenotype, which suggests that certain cases of familial dwarfism may be caused by a mutation of the GSH-1 gene.
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