胚胎干細胞相關轉錄因子1抗體

產品貨號：

BN40431R
中文名稱：

胚胎干細胞相關轉錄因子1抗體
英文名稱：

Rabbit anti-Ecat1 Polyclonal antibody
品牌：

Biorigin

貨號

產品規格

售價

備注
BN40431R-100ul

100ul

￥2360.00

交叉反應：Human 推薦應用：IHC-P,IHC-F,ICC,IF,ELISA
BN40431R-200ul

200ul

￥3490.00

交叉反應：Human 推薦應用：IHC-P,IHC-F,ICC,IF,ELISA

產品描述

英文名稱	Ecat1
中文名稱	胚胎干細胞相關轉錄因子1抗體
別名	C6orf221; Chromosome 6 open reading frame 221; ES cell-associated transcript 1 protein; HYDM2; KHD3L_HUMAN; KHDC3-like protein; KHDC3L.
研究領域	細胞生物干細胞轉錄調節因子
抗體來源	Rabbit
克隆類型	Polyclonal
交叉反應	Human,
產品應用	ELISA=1:5000-10000 IHC-P=1:100-500 IHC-F=1:100-500 ICC=1:100-500 IF=1:100-500 （石蠟切片需做抗原修復） not yet tested in other applications. optimal dilutions/concentrations should be determined by the end user.
分子量	24kDa
細胞定位	細胞核細胞漿
性狀	Liquid
濃度	1mg/ml
免疫原	KLH conjugated synthetic peptide derived from human Ecat1:1-100/217
亞型	IgG
純化方法	affinity purified by Protein A
儲存液	0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
保存條件	Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.
PubMed	PubMed
產品介紹	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 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) [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. SWISS: Q587J8 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.