GIMAP7 抗体 (AA 1-100) (Biotin)
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- 抗原 See all GIMAP7 抗体
- GIMAP7 (GTPase, IMAP Family Member 7 (GIMAP7))
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抗原表位
- AA 1-100
- 适用
- 人
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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 GIMAP7 antibody is conjugated to Biotin
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应用范围
- ELISA, Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
- 预测反应
- Human
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human GIMAP7
- 亚型
- IgG
- Top Product
- Discover our top product GIMAP7 Primary Antibody
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anti-GTPase, IMAP Family Member 7 (GIMAP7) (AA 1-300) antibody
GIMAP7 适用: 人 WB 宿主: 小鼠 Polyclonal unconjugated
anti-GTPase, IMAP Family Member 7 (GIMAP7) (AA 1-273) antibodyGIMAP7 适用: 人 ELISA, WB 宿主: 兔 Polyclonal unconjugated
anti-GTPase, IMAP Family Member 7 (GIMAP7) (N-Term) antibodyGIMAP7 适用: 人 ELISA, WB 宿主: 兔 Polyclonal unconjugated
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- 应用备注
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IHC-P 1:200-400
IHC-F 1:100-500 - 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 for 12 months.
- 有效期
- 12 months
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- 抗原
- GIMAP7 (GTPase, IMAP Family Member 7 (GIMAP7))
- 别名
- GIMAP7 (GIMAP7 产品)
- 别名
- IAN7 antibody, hIAN7 antibody, Ian3 antibody, GTPase, IMAP family member 7 antibody, GIMAP7 antibody, Gimap7 antibody
- 背景
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Synonyms: GTPase IMAP family member 7, hIAN7, IAN 7, IAN7, Immune associated nucleotide, immunity associated nucleotide 7 protein, MGC27027, GIMA7_HUMAN.
Background: The GTPase of the immunity-associated protein (GIMAP) family of proteins include seven members that are expressed by genes residing on human chromosome 7. GIMAP proteins have been implicated in the regulation of lymphomyeloid cell survival. GIMAP7 (GTPase IMAP family member 7), also known as IAN7 (immunity-associated nucleotide 7), is a 300 amino acid protein encoded by a gene that maps to human chromosome 7q36.1. Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia.
- 基因ID
- 168537
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