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锚蛋白重复结构域蛋白11抗体

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产品名称: 锚蛋白重复结构域蛋白11抗体
产品型号: ANKRD11
产品展商: 单克隆抗体/多克隆抗体
产品文档: 无相关文档

简单介绍

锚蛋白重复结构域蛋白11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。锚蛋白重复结构域蛋白11抗体生产每个流程都执行严格的检测标准,保证蛋白抗原产品质量,质量稳定,实验效果明显。


锚蛋白重复结构域蛋白11抗体  的详细介绍

锚蛋白重复结构域蛋白11抗体

规格:1mg/1ml

英文名: ANKRD11

别名: ANCO 1; ANCO1; Ankyrin repeat containing cofactor 1; Ankyrin repeat domain 11; Ankyrin repeat domain containing protein 11; LZ16; T13; ANR11_HUMAN; Ankyrin repeat domain-containing protein 11; Ankyrin

分子量: 296kDa

储存液:Preservative: 15mM Sodium Azide, Constituents: 1% BSA, 0.01M

克隆类型:Polyclonal

亚型:IgG

纯化方法:affinity purified by Protein A

**原:KLH conjugated synthetic peptide derived from human ANKRD11

交叉反应:Human, Mouse, Rat, Dog, Cow, Horse, Sheep,

细胞定位:细胞核

锚蛋白重复结构域蛋白11抗体产品介绍:background: Ankyrin is a membrane protein that mediates the attachment of the erythrocyte membrane skeleton to the plasma membrane and interacts with CD44 and inositol triphosphate. It contains three functional domains: a conserved N-terminal ankyrin repeat domain (ARD(consisting of 22–24 tandem repeats of 33 amino acids), a spectrin binding domain and a variably sized C-terminal regulatory domain. The ankyrin repeat is a 33-residue motif in proteins consisting of two alpha helices separated by loops. It has been studied using multiple sequence alignment to determine which conserved amino acid residues are critical for folding and stability. Ankyrin-repeat proteins have been associated with a number of human diseases; most notably, the cell cycle inhibitor p16 is associated with cancer and the锚蛋白重复结构域蛋白11抗体 Notch protein is a key component of cell signaling pathways whose intracellular repeat domain is disrupted in mutations that give rise to the neurological disorder known as CADASIL. Function: May recruit HDACs to the p160 coactivators/nuclear receptor complex to inhibit ligand-dependent transactivation. Subunit: Interacts with the PAS region of the p160 coactivators. Subcellular Location: Nucleus. DISEASE: 锚蛋白重复结构域蛋白11抗体Defects in ANKRD11 are the cause of KBG syndrome (KBGS) [MIM:148050]. A syndrome characterized by macrodontia of the upper central incisors, distinctive craniofacial findings, short stature, skeletal anomalies, and neurologic involvement that includes global developmental delay, seizures, and intellectual disability. Similarity: Contains 4 ANK repeats. Gene ID: 29123 Database links: Entrez Gene: 29123 Human SwissProt: Q6UB99 Human Unigene: 335003 Human Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.

锚蛋白重复结构域蛋白11抗体产品应用: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:肿瘤  细胞生物  

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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