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范可尼贫血相关蛋白贰抗体

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产物名称: 范可尼贫血相关蛋白贰抗体
产物型号: FANCE
产物展商: 单克隆抗体/多克隆抗体
产物文档: 无相关文档

简单介绍

范可尼贫血相关蛋白贰抗体应用于IHC、WB、 IF、IP、ELISA等科研实验,按理化性质和生物学功能IgM、IgG、IgA、IgE、IgD五类。按抗体的来源,可将其分为天然抗体和**抗体。范可尼贫血相关蛋白贰抗体生产每个流程都执行严格的检测标准,保证蛋白抗原产物质量,质量稳定,实验效果明显。


范可尼贫血相关蛋白贰抗体  的详细介绍

范可尼贫血相关蛋白贰抗体

规格:1尘驳/1尘濒

英文名: FANCE

别名: 2810451D06Rik; AI415634; AW209126; FACE; FAE; FANCE; FANCE_HUMAN; Fanconi anemia complementation group E; Fanconi anemia group E protein; Protein FACE; RGD1561045.

分子量: 59kDa

储存液:0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glyce

克隆类型:笔辞濒测肠濒辞苍补濒

亚型:滨驳骋

纯化方法:affinity purified by Protein A

**原:KLH conjugated synthetic peptide derived from human FANCE

交叉反应:Human, Mouse, Rat, Dog,

细胞定位:细胞核

范可尼贫血相关蛋白贰抗体产物介绍:background: The Fanconi anemia complementation group (FANC) currently includes FANCA, FANCB, FANCC, FANCD1 (also called BRCA2), FANCD2, FANCE, FANCF, FANCG, FANCI, FANCJ (also called BRIP1), FANCL, FANCM and FANCN (also called PALB2). The previously defined group FANCH is the same as FANCA. Fanconi anemia is a genetically heterogeneous recessive disorder characterized by cytogenetic instability, hypersensitivity to DNA crosslinking agents, increased chromosomal breakage, and defective DNA repair. The members of the Fanconi anemia complementation group do not share sequence similarity; they are related by their assembly into a common范可尼贫血相关蛋白贰抗体 nuclear protein complex. This gene encodes the protein for complementation group E. [provided by RefSeq, Jul 2008]. Function: Required for the nuclear accumulation of FANCC and provides a critical bridge between the FA complex and FANCD2. Subunit: Belongs to the multisubunit FA complex composed of FANCA, FANCB, FANCC, FANCE, FANCF, FANCG, FANCL/PHF9 and FANCM. The complex is not found in FA 范可尼贫血相关蛋白贰抗体patients. Interacts with FANCC and FANCD2. Subcellular Location: Nucleus. DISEASE: Defects in FANCE are a cause of Fanconi anemia (FA) [MIM:227650]. FA is a genetically heterogeneous, autosomal recessive disorder characterized by progressive pancytopenia, a diverse assortment of congenital malformations, and a predisposition to the development of malignancies. At the cellular level it is associated with hypersensitivity to DNA-damaging agents, chromosomal instability (increased chromosome breakage), and defective DNA repair. Database links: UniProtKB/Swiss-Prot: Q9HB96.1 Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.

范可尼贫血相关蛋白贰抗体产物应用:WB=1:100-500 ELISA=1:500-1000 IHC-P=1:100-500 IHC-F=1:100-500 ICC=1:100-500 IF=1:100-500 (石蜡切片需做抗原修复) not yet tested in other applications. optimal dilutions/concentrations should be determined by the end user.

研究领域:细胞生物  发育生物学  表观遗传学  

储存条件: Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.

来源: Rabbit

外观: Lyophilized or Liquid


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