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货号: bs-9705R-AF350 基本售价: 2980.0 元 规格: 100ul
产品信息
- 产品编号
- bs-9705R-AF350
- 英文名称
- Anti-ITM2A/AF350
- 中文名称
- AF350标记的完整膜蛋白E25A抗体
- 别 名
- BRICD2A; BRICHOS domain containing 2A; E25 protein; E25A; Integral membrane protein 2A; ITM2A; ITM2A_HUMAN; Protein E25.
- 规格价格
- 100ul/2980元购买 大包装/询价
- 说 明 书
- 100ul
- 研究领域
- 细胞生物 神经生物学 干细胞 细胞周期蛋白 细胞分化
- 抗体来源
- Rabbit
- 克隆类型
- Polyclonal
- 交叉反应
- Human, Mouse, Rat, Pig, Rabbit,
- 产品应用
- IF=1:50-200
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
- 分 子 量
- 30kDa
- 性 状
- Lyophilized or Liquid
- 浓 度
- 1mg/ml
- 免 疫 原
- KLH conjugated synthetic peptide derived from human ITM2A
- 亚 型
- IgG
- 纯化方法
- affinity purified by Protein A
- 储 存 液
- 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol
- 保存条件
- Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. The lyophilized antibody is stable at room temperature for at least one month and for greater than a year when kept at -20°C. When reconstituted in sterile pH 7.4 0.01M PBS or diluent of antibody the antibody is stable for at least two weeks at 2-4 °C.
- 产品介绍
- 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.
Subcellular Location:
Membrane; Single-pass type II membraneprotein (Potential).
Similarity:
Belongs to the ITM2 family.
Contains 1 BRICHOS domain.
Database links:Entrez Gene: 9452 Human
Omim: 300222 Human
SwissProt: O43736 Human
Unigene: 17109 Human
Unigene: 694944 Human
Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.