ITM2A 抗体 (AA 73-123) (AbBy Fluor® 680)
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- 抗原 See all ITM2A 抗体
- ITM2A (Integral Membrane Protein 2A (ITM2A))
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抗原表位
- AA 73-123
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适用
- 人, 小鼠, 大鼠
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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 ITM2A antibody is conjugated to AbBy Fluor® 680
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应用范围
- Western Blotting (WB), Flow Cytometry (FACS), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- 交叉反应
- 人, 小鼠, 大鼠
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human ITM2A
- 亚型
- IgG
- Top Product
- Discover our top product ITM2A Primary Antibody
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- 应用备注
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FCM 1:20-100
IF(IHC-P) 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
- ITM2A (Integral Membrane Protein 2A (ITM2A))
- 别名
- ITM2A (ITM2A 产品)
- 别名
- itm2aa antibody, e25a antibody, itm2ab antibody, bricd2a antibody, BRICD2A antibody, E25A antibody, AW108051 antibody, Bricd2a antibody, E25 antibody, Itm2 antibody, integral membrane protein 2A antibody, integral membrane protein 2A S homeolog antibody, integral membrane protein 2A L homeolog antibody, Integral membrane protein 2A antibody, Itm2a antibody, itm2a.S antibody, ITM2A antibody, itm2a.L antibody, itm2a antibody
- 背景
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Synonyms: E25A, BRICD2A, Integral membrane protein 2A, Protein E25, ITM2A, UNQ603/PRO1189
Background: The type II integral membrane (ITM2) protein family consists of three members ITM2A (also designated E25), ITM2B and ITM2C. ITM2A expression is high in osteogenic and lymphoid tissues, while both ITM2B and ITM2C are expressed in brain. Mutations in the ITM2B gene can lead to familial British dementia (fbd), and autosomal dominant disease characterized by progressive dementia, spasticity, and cerebellar ataxia, or familial Danish dementia (fdd), an autosomal dominant disorder characterized by cataracts, deafness, progressive ataxia, and dementia. The ITM2A 263-amino acid protein contains an N-terminal cytosolic domain, an uncleaved signal anchor sequence, and a tyrosine-rich C-terminal domain. Human ITM2A shares 91 % homology with mouse ITM2A.
- 基因ID
- 9452
- UniProt
- O43736
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