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anti-Human EDNRB Antibodies:
anti-Rat (Rattus) EDNRB Antibodies:
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Human Polyclonal EDNRB Primary Antibody for IHC, IHC (p) - ABIN447514
Park, Mima, Li, Rask-Madsen, He, Mizutani, Katagiri, Maeda, Wu, Khamaisi, Preil, Maddaloni, Sørensen, Rasmussen, Huang, King: Insulin decreases atherosclerosis by inducing endothelin receptor B expression. in JCI insight 2016
Show all 2 Pubmed References
Dog (Canine) Polyclonal EDNRB Primary Antibody for ICC, IHC (p) - ABIN4307017
Comellas, Briva, Dada, Butti, Trejo, Yshii, Azzam, Litvan, Chen, Lecuona, Pesce, Yanagisawa, Sznajder: Endothelin-1 impairs alveolar epithelial function via endothelial ETB receptor. in American journal of respiratory and critical care medicine 2009
Show all 2 Pubmed References
Human Polyclonal EDNRB Primary Antibody for WB - ABIN927147
Ehrenreich, Nau, Dembowski, Hasselblatt, Barth, Hahn, Schilling, Sirén A-L, Brück: Endothelin b receptor deficiency is associated with an increased rate of neuronal apoptosis in the dentate gyrus. in Neuroscience 2000
Cow (Bovine) Polyclonal EDNRB Primary Antibody for IHC, IHC (p) - ABIN441144
Kobayashi, Yoshimoto, Yamamoto, Kimura, Okuda: Roles of EDNs in regulating oviductal NO synthesis and smooth muscle motility in cows. in Reproduction (Cambridge, England) 2016
Dog (Canine) Polyclonal EDNRB Primary Antibody for ICC, IF - ABIN5541800
Tanaka, Sho, Takayama, Wakatsuki, Matsumoto, Migita, Ito, Hamada, Nakajima: Endothelin B receptor expression correlates with tumour angiogenesis and prognosis in oesophageal squamous cell carcinoma. in British journal of cancer 2014
the joint effect of polymorphisms of EDNRB and NOS3 (show NANOS3 Antibodies) on diabetic retinopathy risk was greater than the individual effect of each polymorphism in the analyzed genetic models
the results suggest that aberrant expression of Gli1 (show GLI1 Antibodies) serves a role in HSCR by targeting EDNRB.
Endothelin B receptor (ETBR) is overexpressed in glioblastoma and may be a prognostic marker and useful target for treating cancer patients.
our current findings suggest that human neutrophils display functional ETB receptors with calcium signaling capability, leading to accentuated adhesion to the endothelium.
Endothelin-1 (show EDN1 Antibodies) possesses an anti-apoptotic effect in vascular endothelial cells and this effect is mediated, to a great extent, via the activation of EDNRB, with a minor contribution via activation of EDNRA (show EDNRA Antibodies).
ETBR function contributes to diminished endothelium-dependent dilation in previously preeclamptic women.
ETA and ETB receptors are present in human haemorrhoids with ETB receptors predominating
An IL2 (show IL2 Antibodies)-targeted antibody failed to detect transfected ETB in HEK293 cultures. In contrast, the NT-targeted antibody accurately detected transfected ETB in HEK293 cultures by labeling a 37-kDa band.
In control arteries, ETAR (show EDNRA Antibodies) was expressed by vascular smooth muscle cells in the media whereas ETBR was hardly detected. In giant cell arteritis, both ETAR (show EDNRA Antibodies) and ETBR receptors were expressed by alphaSMA (show ACTA2 Antibodies)-positive cells at the intima-media border. Endothelial cells and inflammatory cells also expressed both ET receptors.
This study concluded that ETB receptors mediate vasodilation in young women, but this effect is lost after menopause.
PDE5 (show PDE5A Antibodies) inhibition and increase in cGMP produce pulmonary vasodilation that is mediated in part through inhibition of the ET pathway, thereby precluding an additional vasodilator effect of ETA/ETB receptor blockade in the presence of PDE5 (show PDE5A Antibodies) inhibition.
ET(A (show EDNRA Antibodies))/ET(B) blockade decreased pulmonary vascular resistance but only during exercise.
endothelial endothelin ET(B) receptors induce NO and EDHF mediated vasodilatation in porcine coronary arteries; in organ culture, endothelial endothelin ET(B) receptors are down-regulated
PKC (show FYN Antibodies) and MAPK (show MAPK1 Antibodies) seem to be involved in the regulation of endothelin type A and type B receptor expression in porcine coronary arteries
extracellular ET-1 (show EDN1 Antibodies) regulates the abundance of ET-1 (show EDN1 Antibodies) mRNA in PAECs, in an ETB receptor-dependent manner, by modulating both mRNA stability and transcription via mechanisms involving receptor endocytosis and both ERK (show MAPK1 Antibodies) and p38 MAPK (show MAPK14 Antibodies) pathways
Hyperinsulinemia caused significant changes in endothelin receptor expression, which suggested that ETR (show EDNRA Antibodies) antagonists might be beneficial for treatment of laminitis in horses.
both ETA and ETB receptors are involved in the net tonic response to ET-1 (show EDN1 Antibodies) in normal laminar veins; a population of ETB receptors may be present on the vascular endothelium and on smooth muscle of laminar veins
Stimulation of ETA and ETB receptors activates native protein kinase C-dependent transient receptor potential channel (TRPC)1 through phospholipid pathways involving phosphoinositol-3,4,5-trisphosphate (PIP)3 and PIP2 in coronary artery myocytes.
ET(B) receptor stimulation relaxes the carbachol precontracted iris sphincter muscle, an effect that is mediated by the ET(B2) receptor subtype, through NO and the release of prostaglandins.
ET-1 (show EDN1 Antibodies) injection into the TG promotes ETAR (show EDNRA Antibodies)/ETBR-mediated facial heat hyperalgesia, and both receptors are clearly implicated in Constriction of infraorbital Nerve-induced hyperalgesia in the murine Trigeminal system.
Altered LAMA1 (show LAMA1 Antibodies) expression in the aganglionic region may contribute to impaired ENCC migration, resulting in HD. These data could help in understanding the pathophysiologic interactions between LAMA1 (show LAMA1 Antibodies) and ENCC migration
Taken together with the finding that ETB R was expressed in Schwann cells, study results demonstrate that endothelin (ET) enhanced neurite outgrowth of neurons mediated by Na(+) /K(+) -ATPase (show ATP1A1 Antibodies) via ETB R in Schwann cells. This study suggests that Na(+) /K(+) -ATPase (show ATP1A1 Antibodies) coupled to the ET-ETB R system plays a critical role in peripheral nerve regeneration via lactate signalling.
ETB receptor signaling is involved in skin sclerosis and in collagen synthesis by dermal fibroblasts
mmLDL increased the serum concentrations and expression of ICAM-1 (show ICAM1 Antibodies) and VCAM-1 (show VCAM1 Antibodies) by activating the ERK1/2 pathway, resulting in the expression of ETB receptors and the enhancement of contractile function in vascular smooth muscle.
ETB receptors in vascular smooth muscle make a small but significant contribution to ETB-dependent regulation of BP. These ETB receptors have no effect on vascular contraction or neointimal remodeling.
Taken together, these data indicate that during high-salt feeding, the autocrine actions of ET-1 (show EDN1 Antibodies) via upregulation of the ETB receptor are critical for IMCD NO production, facilitating inhibition of ion reabsorption.
Wnt (show WNT2 Antibodies)-dependent EdnrB signaling can rescue the defects in melanocyte regeneration caused by Mc1R loss.
we show that ET-1 (show EDN1 Antibodies) acts selectively through EDNRB on astrocytes-and not oligodendrocyte progenitor cells-to indirectly inhibit remyelination.
EDNRB plays a key role in hypoxia tolerance
Differential cell-specific and spatiotemporal expression of the EDN1 system and NOS in the bovine utero-placental unit may be associated with regulation of vascular and cellular functions during pregnancy.
Elevated local expression of ET-1 (show EDN1 Antibodies) and Ednra/Ednrb during the peri (show PLIN1 Antibodies)-ovulatory period induces the high contractile activity of the oviduct to optimize gamete transport.
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.
endothelin B receptor
, endothelin receptor non-selective type
, endothelin receptor subtype B
, endothelin-B receptor
, endothelin ETB receptor
, endothelin receptor B
, endothelin receptor type B