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EDNRB / Endothelin B Receptor  Protein, Antibody, ELISA Kit, cDNA Clone

表達宿主: Human Cells  
15473-H08H-20
15473-H08H-100
20 µg 
100 µg 
Add to Cart
  • Slide 1
表達宿主: Human Cells  
15473-H05H-20
15473-H05H-100
20 µg 
100 µg 
Add to Cart
  • Slide 1

EDNRB / Endothelin B Receptor 相关研究领域

EDNRB / Endothelin B Receptor 相關信號通路

    EDNRB / Endothelin B Receptor 概述&蛋白信息

    EDNRB / Endothelin B Receptor 研究背景

    亞細胞定位: Cell membrane; Multi-pass membrane protein.
    組織特異性: Expressed in placental stem villi vessels, but not in cultured placental villi smooth muscle cells. {ECO:0000269|PubMed:9284755}.
    翻譯後修飾: Palmitoylation of Cys-402 was confirmed by the palmitoylation of Cys-402 in a deletion mutant lacking both Cys-403 and Cys-405. {ECO:0000269|PubMed:9261180}.
    相關疾病 : DISEASE: Waardenburg syndrome 4A (WS4A) [MIM:277580]: 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). {ECO:0000269|PubMed:12189494, ECO:0000269|PubMed:8634719}. Note=The disease is caused by mutations affecting the gene represented in this entry.; DISEASE: Hirschsprung disease 2 (HSCR2) [MIM:600155]: 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. {ECO:0000269|PubMed:8001158, ECO:0000269|PubMed:8630503, ECO:0000269|PubMed:8852659, ECO:0000269|PubMed:8852660}. Note=The disease is caused by mutations affecting the gene represented in this entry.; DISEASE: ABCD syndrome (ABCDS) [MIM:600501]: 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. {ECO:0000269|PubMed:11891690}. Note=The disease is caused by mutations affecting the gene represented in this entry.
    相似的序列: Belongs to the G-protein coupled receptor 1 family. Endothelin receptor subfamily. EDNRB sub-subfamily. {ECO:0000255|PROSITE-ProRule:PRU00521}.
    General information above from UniProt

    EDNRB / Endothelin B Receptor 別稱

    ETB,ET-B,ETBR,ETRB,HSCR,WS4A,ABCDS,ET-BR,HSCR2, [homo-sapiens]
    endothelin receptor type B,EDNRB,RP11-318G21.1,ABCDS,ET-B,ET-BR,ETB,ETBR,ETRB,HSCR,HSCR2,WS4A,endothelin B receptor,endothelin receptor non-selective type, [human]
    endothelin receptor type B,EDNRB,RP11-318G21.1,ABCDS,ET-B,ET-BR,ETB,ETBR,ETRB,HSCR,HSCR2,WS4A,endothelin B receptor,endothelin receptor non-selective type, [mouse]
    ETb,ET-B,ET-BR,ETR-b,Sox10m1, [mus-musculus]

    EDNRB / Endothelin B Receptor 相關文獻

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