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货号： bs-5062R-Cy7 基本售价： 2980.0 元 规格： 100ul
产品信息
- 产品编号
- bs-5062R-Cy7
- 英文名称
- Anti-GNPAT/Cy7
- 中文名称
- Cy7标记的磷酸二羟丙酮酰基转移酶抗体
- 别 名
- DAPAT; DHAPAT; Acyl CoA dihydroxyacetonephosphateacyltransferase; DAP AT; DHAP AT; Dihydroxyacetone phosphate acyltransferase; EC 2.3.1.42; Glyceronephosphate O acyltransferase; OTTHUMP00000036147.
- 规格价格
- 100ul/2980元购买 大包装/询价
- 说 明 书
- 100ul
- 研究领域
- 肿瘤 细胞生物 免疫学 转录调节因子
- 抗体来源
- Rabbit
- 克隆类型
- Polyclonal
- 交叉反应
- Human, Mouse, Rat,
- 产品应用
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
- 分 子 量
- 38, 76kDa
- 性 状
- Lyophilized or Liquid
- 浓 度
- 1mg/ml
- 免 疫 原
- KLH conjugated synthetic peptide derived from human GNPAT
- 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:
GNPAT is a key enzyme located in the peroxisomal membrane which is essential to the synthesis of ether phospholipids. Mutations in GNPAT are associated with rhizomelic chondrodysplasia punctata type 2, which is characterized by rhizomelic shortening of femur and humerus, vertebral disorders, cataract, cutaneous lesions and severe mental retardation.
Subunit:
May be part of an heterotrimeric complex composed of DAP-AT, ADAP-S and a modified form of DAP-AT.
Subcellular Location:
Peroxisome membrane; Peripheral membrane protein; Matrix side. Note=Exclusively localized to the lumenal side of the peroxisomal membrane.
DISEASE:
Defects in GNPAT are the cause of rhizomelic chondrodysplasia punctata type 2 (RCDP2) [MIM:222765]. RDCP2 is characterized by rhizomelic shortening of femur and humerus, vertebral disorders, cataract, cutaneous lesions and severe mental retardation.
Similarity:
Belongs to the GPAT/DAPAT family.
Database links:Entrez Gene: 8443Human
Entrez Gene: 14712Mouse
Omim: 602744Human
SwissProt: O15228Human
SwissProt: P98192Mouse
Unigene: 498028Human
Unigene: 29114Mouse
Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.