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胚胎干细胞相关转录因子1抗体

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产物名称: 胚胎干细胞相关转录因子1抗体
产物型号: Ecat1
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

胚胎干细胞相关转录因子1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。胚胎干细胞相关转录因子1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。


胚胎干细胞相关转录因子1抗体  的详细介绍

胚胎干细胞相关转录因子1抗体

规格:1尘驳/1尘濒

英文名: Ecat1

别名: C6orf221; Chromosome 6 open reading frame 221; ES cell-associated transcript 1 protein; HYDM2; KHD3L_HUMAN; KHDC3-like protein; KHDC3L.

分子量: 24kDa

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 Ecat1

交叉反应:贬耻尘补苍,

细胞定位:细胞核 细胞浆

胚胎干细胞相关转录因子1抗体产物介绍:background: ECAT1 (ES cell-associated transcript 1 protein) is a 217 amino acid protein that belongs to the KHDC1 family. The ECAT1 protein contains an atypical KH domain with amino acid changes at critical sites, suggesting that it may not bind RNA. Expression of ECAT1 appears to be maximal in germinal vesicle oocytes, it tails off through metaphase II oocytes and is undetectable following the completion of the oocyte to embryo transition. Specifically expressed in the oocytes, recent studies suggest that ECAT1 may function as a regulator of genomic imprinting in the oocyte. Defects in ECAT1 are the cause of hydatidiform mole recurrent type胚胎干细胞相关转录因子1抗体 2 (HYDM2), a disorder characterized by excessive trophoblast development that produces a growing mass of tissue inside the uterus at the beginning of a pregnancy. HYDM2 leads to abnormal pregnancies with no embryo, and cystic degeneration of the chorionic villi. Tissue Specificity: Expression appears to be maximal in germinal vesicle oocytes, it tails off through metaphase II oocytes and is undetectable following the completion of the oocyte to embryo transition. DISEASE: Defects in KHDC3L are the cause of hydatidiform mole recurrent type 2 (HYDM2) 胚胎干细胞相关转录因子1抗体[MIM:614293]. A disorder characterized by excessive trophoblast development that produces a growing mass of tissue inside the uterus at the beginning of a pregnancy. It leads to abnormal pregnancies with no embryo, and cystic degeneration of the chorionic villi. Similarity: Belongs to the KHDC1 family. Contains 1 KH domain. Gene ID: 154288 Database links: Entrez Gene: 154288 Human Omim: 611687 Human SwissProt: Q587J8 Human Unigene: 128326 Human Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.

胚胎干细胞相关转录因子1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  干细胞  转录调节因子  

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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