ETBR rabbit pAb

ETBR rabbit pAb

AO-06-ES8504-100

ETBR rabbit pAb 100μL

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Antibody Product Overview

ELK.NoES8504
Product nameETBR rabbit pAb
ReactivityHuman;Rat;Mouse;
ApplicationsWB;IHC;IF;ELISA
Other nameEndothelin B receptor (ET-B;ET-BR;Endothelin receptor non-selective type)
Size100μL
Unit price ($)248
Human gene ID1910
Human Swiss-ProtP24530
SourceRabbit
IsotypeIgG
TargetETBR
Fields>>Calcium signaling pathway;>>cGMP-PKG signaling pathway;>>Neuroactive ligand-receptor interaction;>>Melanogenesis;>>Relaxin signaling pathway;>>Pathways in cancer
Gene nameEDNRB
Protein nameETBR
Human gene linkView Human Gene
Human Swiss linkView Human Swiss-Prot
Mouse gene ID13618
Mouse gene link
Mouse Swiss-ProtP48302
Mouse Swiss linkView Mouse Swiss-Prot
Rat gene ID
Rat gene link
Rat Swiss-Prot
Rat Swiss link
ImmunogenSynthesized peptide derived from ETBR at AA range: 31-80
SpecificityETBR Polyclonal Antibody detects endogenous levels of ETBR
FormulationLiquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
ClonalityPolyclonal
DilutionIHC-p: 100-300.WB 1:500-2000, ELISA 1:10000-20000
PurificationThe antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Concentration1 mg/ml
Storage stability-20°C/1 year
Molecular Weight (Da)
Observed band (KD)50kD
BackgroundThe 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. Alternative splicing and the use of alternative promoters results in multiple transcript variants. [provided by RefSeq, Oct 2016],
Functiondisease:Defects in EDNRB are a cause of Waardenburg syndrome type IV (WS4) [MIM:277580]; also known as Waardenburg-Shah syndrome. WS4 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).,disease: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.,disease:Defects in EDNRB are the cause of Hirschsprung disease type 2 (HSCR2) [MIM:600155]; also known as aganglionic megacolon (MGC). It is a congenital disorder characterized by absence of enteric ganglia along a variable length of the intestine. It is t
Subcellular locationCell membrane ; Multi-pass membrane protein. internalized after activation by endothelins. .
ExpressionExpressed in placental stem villi vessels, but not in cultured placental villi smooth muscle cells.

Additional Images

Image 1
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Western Blot analysis of Hela cells using ETBR Polyclonal Antibody diluted at 1:500. Secondary antibody(catalog#:RS0002) was diluted at 1:20000
Image 2
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Immunohistochemical analysis of paraffin-embedded human-placenta, antibody was diluted at 1:200
Image 3
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Immunohistochemical analysis of paraffin-embedded human-placenta, antibody was diluted at 1:200
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Immunohistochemical analysis of paraffin-embedded Human placenta. 1, Antibody was diluted at 1:200(4° overnight). 2, High-pressure and temperature EDTA, pH8.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 30min).
: AO-06-ES8504-100
: 10 Produits
Hurry! only 10 items left in stock.

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