Anti-EDNRB Antibody |产品详情|进口试剂采购网

您好，欢迎来到拜力生物网站！请登录注册

我的订单 | 联系我们 | 在线客服QQ：3012681483 | 客服电话：400-968-7988 | 工作时间：08:30-17:30

主营产品： ELISA试剂盒、抗体、补体血清、兔补体、干扰素、小鼠测温仪、进口试剂、Quidel代理、Swant代理、PBL Assay Science代理

网站首页产品中心代理品牌新闻资讯资源中心关于我们

所在位置：首页 > 产品中心 > Antibodies > Antibodies产品

订购信息

上海拜力生物科技公司

Tel:400-968-7988 021-33779008

Anti-EDNRB Antibody

品牌：Antibodies

货号：

规格：50µl

货期：

应用：

咨询客服

立即购买加入购物车

Anti-EDNRB Antibody

商品详情参考文献相关资料

Overview

Name:	Anti-EDNRB Antibody See all EDNRB primary antibodies
Description:	Rabbit polyclonal antibody to EDNRB
Specificity:	EDNRB pAb detects endogenous levels of EDNRB protein.
Applications:	WB, IHC
Reactivity:	Human, Mouse
Immunogen:	Recombinant full length Human EDNRB.
Host:	Rabbit
Clonality:	Polyclonal
Conjugate:	Unconjugated
Molecular Weight:	~50 kDa
Purity:	The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen and the purity is > 95% (by SDS-PAGE).
Product Form:	1mg/ml in PBS?with?0.1%?Sodium?Azide,?50%?Glycerol.

Target

Function:	Non-specific receptor for endothelin 1, 2, and 3. Mediates its action by association with G proteins that activate a phosphatidylinositol-calcium second messenger system.
Tissue Specificity:	Expressed in placental stem villi vessels, but not in cultured placental villi smooth muscle cells.
Involvement in Disease:	Waardenburg syndrome 4A: A disorder characterized by the association of Waardenburg features (depigmentation and deafness) with the absence of enteric ganglia in the distal part of the intestine (Hirschsprung disease). Hirschsprung disease 2: A disorder of neural crest development characterized by absence of enteric ganglia along a variable length of the intestine. It is the most common cause of congenital intestinal obstruction. Early symptoms range from complete acute neonatal obstruction, characterized by vomiting, abdominal distention and failure to pass stool, to chronic constipation in the older child. ABCD syndrome: An autosomal recessive syndrome characterized by albinism, black lock at temporal occipital region, bilateral deafness, aganglionosis of the large intestine and total absence of neurocytes and nerve fibers in the small intestine.
Sequence Similarities:	Belongs to the G-protein coupled receptor 1 family. Endothelin receptor subfamily. EDNRB sub-subfamily.
Post-Translational Modification:	Palmitoylation of Cys-402 was confirmed by the palmitoylation of Cys-402 in a deletion mutant lacking both Cys-403 and Cys-405.
Cellular Location:	Cell membrane.
Database Links:	Entrez Gene: 1910?Human Entrez Gene: 13618?Mouse Omim: 131244?Human SwissProt: P24530?Human SwissProt: P48302?Mouse Unigene: 82002?Human Unigene: 229532?Mouse
Synonyms:	ABCDS Antibody Ednra Antibody EDNRB Antibody EDNRB_HUMAN Antibody Endothelin B Receptor Antibody Endothelin B receptor precursor Antibody Endothelin receptor Non selective type Antibody Endothelin receptor non-selective type Antibody Endothelin receptor type B Antibody ET B Antibody ET-B Antibody ET-BR Antibody ETB Antibody ETBR Antibody ETRB Antibody Hirschsprung disease 2 Antibody HSCR Antibody HSCR2 Antibody OTTHUMP00000018534 Antibody OTTHUMP00000178736 Antibody WS4A Antibody
Information:	Target information shown above is from the UniProt Consortium.