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Endothelin B Receptor Rabbit pAb (bs-4198R)  
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產品編號 bs-4198R
英文名稱 Endothelin B Receptor Rabbit pAb
中文名稱 內皮素B受體抗體
別    名 ABCDS; Ednra; Ednrb; EDNRB_HUMAN; Endothelin B receptor; Endothelin B receptor precursor; Endothelin receptor Non selective type; Endothelin receptor non-selective type; Endothelin receptor type B; ET B; ET-B; ET-BR; ETB; ETRB; Hirschsprung disease 2; HSCR; HSCR2; EDNRB; HSCR; WS4A.  
Specific References  (4)     |     bs-4198R has been referenced in 4 publications.
[IF=10.787] Ravi Kumar. et al. Induction of reactive oxygen species by mechanical stretch drives endothelin production in neonatal pig renal epithelial cells. REDOX BIOL. 2022 Sep;55:102394  WB ;  Pig.  
[IF=4.757] Nataliia Hula. et al. The Long-Term Effects of Prenatal Hypoxia on Coronary Artery Function of the Male and Female Offspring. BIOMEDICINES. 2022 Dec;10(12):3019  IF ;  Rat.  
[IF=2.107] Ji L et al. A high affinity nanobody against endothelin receptor type B: a new approach to the treatment of melanoma. Mol Biol Rep. 2020 Mar;47(3):2137-2147.  WB ;  Human.  
[IF=0.939] Prayitnaningsih et al. Neuropathy optic glaucomatosa induced by systemic hypertension through activation endothelin-1 signaling pathway in central retinal artery in rats. (2016) Int.J.Ophthalmol. 9:1568-1577  IF(IHC-P) ;  Rat.  
研究領域 心血管  免疫學  信號轉導  G蛋白偶聯受體  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 Human,Mouse,Rat (predicted: Rabbit,Pig,Cow,Chicken,Dog,Horse)
產品應用 WB=1:500-2000
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
理論分子量 47 kDa
檢測分子量
細胞定位 細胞膜 
性    狀 Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human Endothelin B Receptor: 378-442/442 <Cytoplasmic>
亞    型 IgG
純化方法 affinity purified by Protein A
緩 沖 液 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
保存條件 Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles.
注意事項 This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
PubMed PubMed
產品介紹 The protein encoded by this gene is a G protein-coupled receptor which activates a phosphatidylinositol-calcium second messenger system. Its ligand, endothelin, consists of a family of three potent vasoactive peptides: ET1, ET2, and ET3. Studies suggest that the multigenic disorder, Hirschsprung disease type 2, is due to mutations in the endothelin receptor type B gene. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq].

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.

Subcellular Location:
Cell membrane; Multi-pass membrane protein.

Tissue Specificity:
Expressed in placental stem villi vessels, but not in cultured placental villi smooth muscle cells.

Post-translational modifications:
Palmitoylation of Cys-402 was confirmed by the palmitoylation of Cys-402 in a deletion mutant lacking both Cys-403 and Cys-405.

DISEASE:
Defects in EDNRB are a cause of Waardenburg syndrome type 4A (WS4A) [MIM:277580]; also known as Waardenburg-Shah syndrome. WS4A is characterized by the association of Waardenburg features (depigmentation and deafness) and the absence of enteric ganglia in the distal part of the intestine (Hirschsprung disease).
Defects in EDNRB are the cause of Hirschsprung disease type 2 (HSCR2) [MIM:600155]; also known as aganglionic megacolon (MGC). HSCR2 is a congenital disorder 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.
Defects in EDNRB are the cause of ABCD syndrome (ABCDS) [MIM:600501]. ABCD syndrome is 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.

Similarity:
Belongs to the G-protein coupled receptor 1 family. Endothelin receptor subfamily. EDNRB sub-subfamily.

SWISS:
P24530

Gene ID:
1910

Database links:

Entrez Gene: 408082 Chicken

Entrez Gene: 281750 Cow

Entrez Gene: 100033875 Horse

Entrez Gene: 1910 Human

Entrez Gene: 13618 Mouse

Entrez Gene: 100009477 Rabbit

Entrez Gene: 50672 Rat

Omim: 131244 Human

SwissProt: P28088 Cow

SwissProt: O62709 Horse

SwissProt: P24530 Human

SwissProt: P48302 Mouse

SwissProt: P35463 Pig

SwissProt: Q9N0W7 Rabbit

SwissProt: P21451 Rat

Unigene: 487 Cow

Unigene: 13045 Horse

Unigene: 82002 Human

Unigene: 229532 Mouse

Unigene: 27603 Pig

Unigene: 6857 Rabbit

Unigene: 11412 Rat



產品圖片
Sample: Lane1:Heart (Rat)Lysate at 40 ug Lane2:Heart (Mouse) Lysate at 40 ug Primary: Anti-Endothelin B Receptor(bs-4198R)at 1/300 dilution Secondary: IRDye800CW Goat Anti-RabbitIgG at 1/20000 dilution Predicted band size: 47kD Observed band size: 50kD
Sample: Lane 1: Embryo (Mouse) Tissue Lysate at 40 ug Lane 2: Lung (Mouse) TissueLysate at 40 ug Lane 3: Cerebrum (Mouse) Tissue Lysate at 40 ug Lane 4: Cerebrum (Rat) Tissue Lysate at 40 ug Lane 5: A431 (Human) Cell Lysate at 30 ug Lane 6: BV-2 (Mouse) Cell Lysate at 30 ug Lane 7: SH-SY5Y (Human) Cell Lysate at 30 ug Primary: Anti-Endothelin B Receptor (bs-4198R) at 1/500 dilution Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution Predicted band size: 47 kD Observed band size: 50 kD
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