GIMAP8 抗体 (AA 551-565) (HRP)
Quick Overview for GIMAP8 抗体 (AA 551-565) (HRP) (ABIN898933)
抗原
See all GIMAP8 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 551-565
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交叉反应
- 小鼠
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预测反应
- Human,Rat,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 GIMAP8
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亚型
- IgG
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anti-GTPase, IMAP Family Member 8 (GIMAP8) (AA 1-300) antibody
GIMAP8 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
anti-GTPase, IMAP Family Member 8 (GIMAP8) (N-Term) antibodyGIMAP8 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
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应用备注
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WB 1:300-5000
IHC-P 1:200-400
IHC-F 1:100-500 -
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
- Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % 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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注意事项
- Do NOT add Sodium Azide! Use of Sodium Azide will inhibit enzyme activity of horseradish peroxidase.
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储存条件
- -20 °C
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储存方法
- Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
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有效期
- 12 months
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- GIMAP8 (GTPase, IMAP Family Member 8 (GIMAP8))
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别名
- GIMAP8
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背景
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Synonyms: GTPase IMAP family member 8, hIAN6, Human immune associated nucleotide 6, IAN9, IANT, Immune associated nucleotide, Immune-associated nucleotide-binding protein 9, Protein IanT, GIMA8_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. GIMAP8, also known as IAN9 (immune-associated nucleotide-binding protein 9) or IANT, is a 665 amino acid protein that localizes to Golgi apparatus, Endoplasmic reticulum and mitochondria. Suggested to have an anti-apoptotic effect on the immune system, GIMAP8 plays a role in infection response and is encoded by a gene that maps to human chromosome 7q36.1. 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
- 155038
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UniProt
- Q8ND71
抗原
-
