GTPase, IMAP Family Member 1 (GIMAP1) (AA 31-130) 抗体
Quick Overview for GTPase, IMAP Family Member 1 (GIMAP1) (AA 31-130) 抗体 (ABIN873318)
抗原
See all GTPase, IMAP Family Member 1 (GIMAP1) 抗体适用
宿主
克隆类型
标记
应用范围
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抗原表位
- AA 31-130
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交叉反应
- 大鼠
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预测反应
- Human,Mouse,Horse,Rabbit
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纯化方法
- Purified by Protein A.
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免疫原
- KLH conjugated synthetic peptide derived from human GIMAP1
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亚型
- IgG
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anti-GTPase, IMAP Family Member 1 (GIMAP1) (N-Term) antibody
GIMAP1 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
anti-GTPase, IMAP Family Member 1 (GIMAP1) (N-Term) antibodyGIMAP1 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
anti-GTPase, IMAP Family Member 1 (GIMAP1) (N-Term) antibodyGIMAP1 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
anti-GTPase, IMAP Family Member 1 (GIMAP1) antibodyGIMAP1 适用: 人 WB, ELISA 宿主: 兔 Polyclonal unconjugated
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应用备注
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ELISA 1:500-1000
IHC-P 1:200-400
IHC-F 1:100-500
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
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浓度
- 1 μg/μL
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缓冲液
- 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.
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储存液
- ProClin
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注意事项
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
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储存条件
- 4 °C,-20 °C
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储存方法
- Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.
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有效期
- 12 months
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- GTPase, IMAP Family Member 1 (GIMAP1)
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别名
- Gimap1
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背景
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Synonyms: GIMA1_HUMAN, GIMAP1, GTPase IMAP family member 1, hIMAP1, Immunity-associated protein 1.
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. GIMAP1 (GTPase, IMAP family member 1), also known as IMAP1 (immunity-associated protein 1), HIMAP1 or IMAP38, is a 306 amino acid single-pass type IV membrane protein of the endoplasmic reticulum (ER) belonging to the GIMAP family. Encoded by a gene located on human chromosome 7, GIMAP1 is expressed primarily in spleen with lower levels found in lymph node. Chromosome 7 houses over 1,000 genes, comprises nearly 5 % of the human genome and has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome.
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基因ID
- 170575
抗原
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