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Recombinant Human EDNRB/ETRB Protein, N-GST & C-His

Catalog #:   YHD63001 Specific References (136) DATASHEET
Applications: ELISA, Immunogen, SDS-PAGE, WB, Bioactivity testing in progress
Expression system: E. coli
Accession: P24530
Protein length: Glu236-Thr271
Overview

Catalog No.

YHD63001

Expression system

E. coli

Species

Homo sapiens (Human)

Protein length

Glu236-Thr271

Predicted molecular weight

32.42 kDa

Nature

Recombinant

Endotoxin level

Please contact with the lab for this information.

Purity

>90% as determined by SDS-PAGE.

Accession

P24530

Applications

ELISA, Immunogen, SDS-PAGE, WB, Bioactivity testing in progress

Form

Lyophilized

Storage buffer

Lyophilized from a solution in PBS pH 7.4, 0.02% NLS, 1mM EDTA, 4% Trehalose, 1% Mannitol.

Reconstitution

Reconstitute in sterile water for a stock solution. A copy of datasheet will be provided with the products, please refer to it for details.

Shipping

In general, proteins are provided as lyophilized powder/frozen liquid. They are shipped out with dry ice/blue ice unless customers require otherwise.

Stability and Storage

Use a manual defrost freezer and avoid repeated freeze thaw cycles. Store at 2 to 8°C for frequent use. Store at -20 to -80°C for twelve months from the date of receipt.

Alternative Names

Endothelin receptor type B, EDNRB, ETRB, ET-BR, Endothelin receptor non-selective type, ET-B

Data Image
  • SDS-PAGE
    SDS PAGE for Recombinant Human EDNRB/ETRB protein
References

Endothelin receptor B inhibition triggers apoptosis and enhances angiogenesis in melanomas. PMID: 15604257

Endothelin receptor B is required for the expansion of melanocyte precursors and malignant melanoma. PMID: 15906230

Endothelin-1 down-regulates matrix metalloproteinase 14 and 15 expression in human first trimester trophoblasts via endothelin receptor type B. PMID: 27864359

Endothelin-1 promotes human germinal vesicle-stage oocyte maturation by downregulating connexin-26 expression in cumulus cells. PMID: 29126233

EDNRB/EDN3 and Hirschsprung disease type II. PMID: 11434563

Prognostic values of EDNRB in triple-negative breast cancer. PMID: 32934717

Review and update of mutations causing Waardenburg syndrome. PMID: 20127975

Ednrb -/- mice with hirschsprung disease are missing Gad2-expressing enteric neurons in the ganglionated small intestine. PMID: 35959491

Waardenburg Syndrome. PMID: 32809714

Waardenburg syndrome. PMID: 9279758

EDNRB Reverses Methylprednisolone-Mediated Decrease in Neural Progenitor Cell Viability via Regulating PI3K/Akt Pathway and lncRNA Expression. PMID: 31760579

News from the endothelin-3/EDNRB signaling pathway: Role during enteric nervous system development and involvement in neural crest-associated disorders. PMID: 30171849

Associations of EDNRA and EDNRB Polymorphisms with Intracerebral Hemorrhage. PMID: 31150867

Role of endothelin receptor type B (EDNRB) in lung adenocarcinoma. PMID: 32394530

A gene regulatory network explains RET-EDNRB epistasis in Hirschsprung disease. PMID: 31313802

Unraveling molecular mechanisms of head and neck cancer. PMID: 35932993

EDNRB isoform 3 confers Temozolomide resistance in A375 melanoma cells by modulating membrane potential, reactive oxygen species and mitochondrial Ca2. PMID: 31496797

The heterozygous EDNRB mutation in a Chinese family with Waardenburg syndrome type I. PMID: 31544051

EDNRB gene variants and melanoma risk in two southern European populations. PMID: 21507037

High-altitude adaptation in humans: from genomics to integrative physiology. PMID: 28951950

KIF1A and EDNRB are differentially methylated in primary HNSCC and salivary rinses. PMID: 20162572

Glial Cell-Derived Neurotrophic Factor Induces Enteric Neurogenesis and Improves Colon Structure and Function in Mouse Models of Hirschsprung Disease. PMID: 32687927

Novel variants in EDNRB gene in Waardenburg syndrome type II and SOX10 gene in PCWH syndrome. PMID: 33234331

Hypermethylation of EDNRB promoter contributes to the risk of colorectal cancer. PMID: 24326135

EDNRB and DCC salivary rinse hypermethylation has a similar performance as expert clinical examination in discrimination of oral cancer/dysplasia versus benign lesions. PMID: 23637120

EDNRB mutations cause Waardenburg syndrome type II in the heterozygous state. PMID: 28236341

[Hereditary hypomelanocytoses: the role of PAX3, SOX10, MITF, SNAI2, KIT, EDN3 and EDNRB genes]. PMID: 24379252

Methylation analysis of EDNRB in human colon tissues of Hirschsprung's disease. PMID: 23579558

EdnrB Governs Regenerative Response of Melanocyte Stem Cells by Crosstalk with Wnt Signaling. PMID: 27134165

E. coli JM83 damages the mucosal barrier in Ednrb knockout mice to promote the development of Hirschsprung‑associated enterocolitis via activation of TLR4/p‑p38/NF‑κB signaling. PMID: 35302172

Lymphopenia in Ednrb-deficient rat was strongly modified by genetic background. PMID: 22975636

Single-cell RNA-sequencing analyses identify heterogeneity of CD8+ T cell subpopulations and novel therapy targets in melanoma. PMID: 33575475

Andrographolide Promotes Interaction Between Endothelin-Dependent EDNRA/EDNRB and Myocardin-SRF to Regulate Pathological Vascular Remodeling. PMID: 35127859

Transcriptomic analysis and ednrb expression in cochlear intermediate cells reveal developmental differences between inner ear and skin melanocytes. PMID: 33484097

The effect of miR-124-3p on cell proliferation and apoptosis in bladder cancer by targeting EDNRB. PMID: 31572460

Homozygous EDNRB mutation in a patient with Waardenburg syndrome type 1. PMID: 28502583

CD31, EDNRB and TSPAN7 are promising prognostic markers in clear-cell renal cell carcinoma revealed by genome-wide expression analyses of primary tumors and metastases. PMID: 22213152

Genetic heterogeneity in GJB2, COL4A3, ATP6V1B1 and EDNRB variants detected among hearing impaired families in Morocco. PMID: 35301649

Hypoxic regulation of EDN1, EDNRA, EDNRB, and ECE1 gene expressions in ERN1 knockdown U87 glioma cells. PMID: 31734650

Identification of nine novel variants across PAX3, SOX10, EDNRB, and MITF genes in Waardenburg syndrome with next-generation sequencing. PMID: 36331148

Aberrant promoter methylation of EDNRB in lung cancer in Taiwan. PMID: 16328051

Low expression of endothelin receptor B (EDNRB) is related to H3K9me3 binding with the EDNRB promoter region and is associated with the clinical T tumor stage in salivary adenoid cystic carcinoma. PMID: 26166030

Quantitative analysis of promoter methylation of the EDNRB gene in gastric cancer. PMID: 21264540

Epigenetic and genetic alterations of the EDNRB gene in nasopharyngeal carcinoma. PMID: 18187958

Promoter hypermethylation of the EDNRB gene in nasopharyngeal carcinoma. PMID: 11920632

Identification of aberrant promoter methylation of EDNRB gene in esophageal squamous cell carcinoma. PMID: 18564167

c-Ret-mediated hearing losses. PMID: 22295143

Clinical relationship between EDN-3 gene, EDNRB gene and Hirschsprung's disease. PMID: 14669347

Adamdec1, Ednrb and Ptgs1/Cox1, inflammation genes upregulated in the intestinal mucosa of obese rats, are downregulated by three probiotic strains. PMID: 28512356

New test for endothelin receptor type B (EDNRB) mutation genotyping in horses. PMID: 27039359

Identification of aberrantly methylated differentially expressed genes and associated pathways in endometrial cancer using integrated bioinformatic analysis. PMID: 32170852

Expression of endothelin type B receptors (EDNRB) on smooth muscle cells is controlled by MKL2, ternary complex factors, and actin dynamics. PMID: 30332284

Phenotype variation in two-locus mouse models of Hirschsprung disease: tissue-specific interaction between Ret and Ednrb. PMID: 12574515

Molecular characterization of four induced alleles at the Ednrb locus. PMID: 9371807

Interactions between Sox10 and EdnrB modulate penetrance and severity of aganglionosis in the Sox10Dom mouse model of Hirschsprung disease. PMID: 15294878

Cloning and association analysis of KIT and EDNRB polymorphisms with dominant white coat color in the Chinese raccoon dog (Nyctereutes procyonoides procyonoides). PMID: 26125860

Heterozygous endothelin receptor B (EDNRB) mutations in isolated Hirschsprung disease. PMID: 8852660

High-incidence spontaneous tumors in JF1/Ms mice: relevance of hypomorphic germline mutation and subsequent promoter methylation of Ednrb. PMID: 24194353

Re-expression of the methylated EDNRB gene in oral squamous cell carcinoma attenuates cancer-induced pain. PMID: 21782343

LncRNA TGFB2-AS1 regulates lung adenocarcinoma progression via act as a sponge for miR-340-5p to target EDNRB expression. PMID: 32774737

Aberrant methylation of EDNRB and p16 genes in hepatocellular carcinoma (HCC) in Taiwan. PMID: 16391877

A deletion in the intergenic region upstream of Ednrb causes head spot in the rat strain KFRS4/Kyo. PMID: 28356074

RET and EDNRB mutation screening in patients with Hirschsprung disease: Functional studies and its implications for genetic counseling. PMID: 26395553

Epilation induces hair and skin pigmentation through an EDN3/EDNRB-dependent regenerative response of melanocyte stem cells. PMID: 28779103

Coexpression of recombinant adenovirus carrying GDNF and EDNRB genes in neural stem cells in vitro. PMID: 23504906

QTL analysis identifies a modifier locus of aganglionosis in the rat model of Hirschsprung disease carrying Ednrb(sl) mutations. PMID: 22132166

Endothelin receptor B (EDNRB) is not the causative gene of the English spotting locus in the domestic rabbit (Oryctolagus cuniculus). PMID: 20497153

New roles of EDNRB and EDN3 in the pathogenesis of Hirschsprung disease. PMID: 20009762

Interactions between Sox10, Edn3 and Ednrb during enteric nervous system and melanocyte development. PMID: 16650841

Significant Association of rs2147555 Genetic Polymorphism in the EDNRB Gene with Hirschsprung Disease in Southern Chinese Children. PMID: 33178831

Aberrant methylated EDNRB can act as a potential diagnostic biomarker in sporadic colorectal cancer while KISS1 is controversial. PMID: 28140749

Exclusion of EDNRB and KIT as the basis for white spotting in Border Collies. PMID: 11178229

The immunosuppressive role of Edn3 overexpression in the melanoma microenvironment. PMID: 34288510

Genetic variation in the GDNF promoter affects its expression and modifies the severity of Hirschsprung's disease (HSCR) in rats carrying Ednrb(sl) mutations. PMID: 26318480

Apolipoprotein B is a new target of the GDNF/RET and ET-3/EDNRB signalling pathways. PMID: 22897442

New variations of the EDNRB gene and its association with sporadic Hirschsprung's disease in Korea. PMID: 17011274

Polymorphisms of EDNRB, ATG, and ACE genes in salt-sensitive hypertension. PMID: 18758497

Association of endothelin-beta receptor (EDNRB) gene variants in anorectal malformations. PMID: 17618893

Endothelin receptor B enhances liver injury and pro-inflammatory responses by increasing G-protein-coupled receptor kinase-2 expression in primary biliary cholangitis. PMID: 36396948

Genetic association study of endothelin-1 and its receptors EDNRA and EDNRB in migraine with aura. PMID: 19558538

Genetic evidence does not support direct regulation of EDNRB by SOX10 in migratory neural crest and the melanocyte lineage. PMID: 16412618

Novel Neuropathic Pain Mechanisms Associated With Allergic Inflammation. PMID: 31920952

Altered neuronal density and neurotransmitter expression in the ganglionated region of Ednrb null mice: implications for Hirschsprung's disease. PMID: 23360229

The Genetics of Deafness in Domestic Animals. PMID: 26664958

Sacral neural crest-derived cells enter the aganglionic colon of Ednrb-/- mice along extrinsic nerve fibers. PMID: 21858821

Upregulation of PSCDBP, TLR2, TWIST1, FLJ35382, EDNRB, and RGS12 gene expression in human myometrium at labor. PMID: 18497345

Acetylcholine from tuft cells promotes M2 macrophages polarization in Hirschsprung-associated enterocolitis., PMID:40416975

Structure of a lasso peptide bound ETB receptor provides insights into the mechanism of GPCR inverse agonism., PMID:40263271

Understanding metabolic characteristics and molecular mechanisms of large to giant congenital melanocytic nevi: implications for melanoma risk and therapeutic targets., PMID:40190193

Epigenetic alteration of smooth muscle cells regulates endothelin-dependent blood pressure and hypertensive arterial remodeling., PMID:40146226

Novel genetic determinants contribute to hearing loss in a central European cohort with enlarged vestibular aqueduct., PMID:40121402

Enteric neural crest development in Astyanax mexicanus surface fish and cavefish., PMID:40060476

Identification of potential biomarkers for lung cancer using integrated bioinformatics and machine learning approaches., PMID:40014586

The Impact of Mutant EDNRB on the Two-End Black Coat Color Phenotype in Chinese Local Pigs., PMID:40002960

Aberrant DNA methylation of EDNRB, MGMT and TIMP3 gene promoters in saliva of head and neck carcinoma patients as a diagnostic tool., PMID:39847241

Construction of the bromodomain-containing protein-associated prognostic model in triple-negative breast cancer., PMID:39827145

EDNRB negatively regulates glycolysis to exhibit anti-tumor functions in prostate cancer by cGMP/PKG pathway., PMID:39788311

Short-term estradiol administration does not restore endothelin-B receptor-mediated vasodilation in postmenopausal women., PMID:39773019

Fructo-Oligosaccharides Enhance the Expression of Genes Related to Focal Adhesion- and Inflammation-Pathways in Small Intestinal Absorptive Caco-2 Cells., PMID:39756968

Microglial cell proliferation is regulated, in part, by reactive astrocyte ETBR signaling after ischemic stroke., PMID:39716588

[Molecular mechanism of Xiangsha Liujunzi Decoction in treating chronic atrophic gastritis based on transcriptome sequencing technology]., PMID:39701680

Lineage-specific intersection of endothelin and GDNF signaling in enteric nervous system development., PMID:39641974

The Ednrb-Aim2-AKT axis regulates neural crest-derived melanoblast proliferation during early development., PMID:39555938

Angiopoietin-1 attenuates lipopolysaccharide-induced endotoxemia in a Hirschsprung's disease murine model by improving intestinal vascular integrity: implications for treating postoperative Hirschsprung-associated enterocolitis., PMID:39466437

Enhancement of enteric neural stem cell neurogenesis by glial cell-derived neurotrophic factor in experimental Hirschsprung's disease., PMID:39460767

Right Ventricular Hypertrophy in Spontaneously Hypertensive Rats (SHR/NHsd) Is Associated with Inter-Individual Variations of the Pulmonary Endothelin System., PMID:39452062

Structure of endothelin ETB receptor-Gi complex in a conformation stabilized by unique NPxxL motif., PMID:39414992

Identification of immune-related hub genes in spinal cord injury., PMID:39367463

An iron-rich subset of macrophages promotes tumor growth through a Bach1-Ednrb axis., PMID:39347789

Mechanism of Mongolian mind-body interactive therapy in regulating essential hypertension through HTR2B: A metabolome- and transcriptome-based study., PMID:39319128

Genomic analyses of intricate interaction of TE-lncRNA overlapping genes with miRNAs in human diseases., PMID:39215947

Endothelin 3/EDNRB signaling induces thermogenic differentiation of white adipose tissue., PMID:39174539

Adipocyte endothelin B receptor activation inhibits adiponectin production and causes insulin resistance in obese mice., PMID:39096077

Molecular mechanism of the endothelin receptor type B interactions with Gs, Gi, and Gq., PMID:39043181

Enteric neural stem cell transplant restores gut motility in mice with Hirschsprung disease., PMID:39042470

Comprehensive analysis of the endothelin system in the kidneys of mice, rats, and humans., PMID:38904098

Microarray analysis demonstrates up-regulation of the endothelin-1 gene with compensatory down-regulation of the ETA receptor gene in human portal vein., PMID:38860875

Discovery and technical validation of high-performance methylated DNA markers for the detection of cervical lesions at risk of malignant progression in low- and middle-income countries., PMID:38643219

Methylation analysis of DCC gene in saliva samples is an efficient method for non-invasive detection of superficial hypopharyngeal cancer., PMID:38538728

Mesenchymal Stem Cells Attenuates Hirschsprung diseases - Associated Enterocolitis by Reducing M1 Macrophages Infiltration via COX-2 Dependent Mechanism., PMID:38508971

Identification of new subtypes and potential genetic signatures in triple-negative breast cancer using weighted gene co-expression network analysis., PMID:38305604

Enhanced quality of hESC-derived melanocytes through modified concentration of endothelin-1., PMID:38284190

Refining breast cancer biomarker discovery and drug targeting through an advanced data-driven approach., PMID:38253993

High incidence of EDNRB gene mutation in seven southern Chinese familial cases with Hirschsprung's disease., PMID:38253735

Putative role of endothelin receptor B in the development and maintenance of taste buds within the circumvallate papillae., PMID:38220089

EDNRB inhibits the growth and migration of prostate cancer cells by activating the cGMP-PKG pathway., PMID:38205153

Genome-wide DNA methylation of lesional and peri-lesional skin in vitiligo: a comparative and integrated analysis of multi-omics in Chinese population., PMID:38182908

Genome-wide detection of selection signatures in Jianli pigs reveals novel cis-regulatory haplotype in EDNRB associated with two-end black coat color., PMID:38166718

Activation of ETAR and ETBR in myocardial tissue characterizes heart failure induced by experimental autoimmune myocarditis., PMID:38166688

Endothelin receptor B-deficient mice are protected from high-fat diet-induced metabolic syndrome., PMID:38159882

Multiple gene-drug prediction tool reveals Rosiglitazone based treatment pathway for non-segmental vitiligo., PMID:38159176

The mechanisms underlying alcohol-induced decreased splenic size: A network meta-analysis study., PMID:38059389

RET enhancer haplotype-dependent remodeling of the human fetal gut development program., PMID:37948459

ET-1 receptor type B (ETBR) overexpression associated with ICAM-1 downregulation leads to inflammatory attenuation in experimental autoimmune myocarditis., PMID:37901475

Suppression of PGE2/EP2 signaling alleviates Hirschsprung disease by upregulating p38 mitogen-activated protein kinase activity., PMID:37522903

Apoptosis Related Human Wharton's Jelly-Derived Stem Cells Differentiation into Osteoblasts, Chondrocytes, Adipocytes and Neural-like Cells-Complete Transcriptomic Assays., PMID:37373173

Datasheet
$ 313
Product specifications
100 μg 313 1 mg 1629

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Recombinant Human EDNRB/ETRB Protein, N-GST & C-His [YHD63001]
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