欧美一区二区三区久久综,大象视频入口一二三2021,色婷婷导航

您好，歡迎來到拜力生物網站！請登錄注冊

我的訂單 | 聯系我們 | 在線客服QQ：3012681483 | 客服電話：400-968-7988 | 工作時間：08:30-17:30

主營產品： ELISA試劑盒、抗體、補體血清、兔補體、干擾素、小鼠測溫儀、進口試劑、Quidel代理、Swant代理、PBL Assay Science代理

網站首頁產品中心代理品牌新聞資訊資源中心關于我們

所在位置：首頁 > 產品中心 > Antibodies > Antibodies產品

訂購信息

上海拜力生物科技公司

Tel:400-968-7988 021-33779008

Anti-EDNRB Antibody

品牌：Antibodies

貨號：

規(guī)格：50μl

貨期：

應用：

咨詢客服

立即購買加入購物車

Anti-EDNRB Antibody

商品詳情參考文獻相關資料

Overview

Name:	Anti-EDNRB Antibody See all EDNRB primary antibodies
Description:	Rabbit polyclonal antibody to EDNRB
Specificity:	The antibody detects endogenous level of total EDNRB protein.
Applications:	E, WB, IHC
Reactivity:	Human
Immunogen:	Synthetic peptide peptide corresponding to a region derived from 70-84 amino acids of human endothelin receptor type B
Host:	Rabbit
Clonality:	Polyclonal
Conjugate:	Unconjugated
Formulation:	Supplied at 1mg / mL in phosphate buffered saline (without Mg2+ and Ca2+), pH 7.3, 0.05% sodium azide and 50% glycerol.
Storage:	Store at -20?C / 1 year

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 Omim: 131244?Human SwissProt: P24530?Human Unigene: 82002?Human
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.