Recommended
product-img
  • Products
  • Discover MP Targets
  • Discover Research Areas
  • mProX™ Human EDNRB Stable Cell Line

    [CAT#: S01YF-0923-PY65]
    Product Category:
    Membrane Protein Stable Cell Lines
    Subcategory:
    GPCR Cell Lines

    Datasheet MSDS Request COA

    Certificate of Analysis Lookup
    To download a Certificate of Analysis, please enter a lot number in the search box below. Note: Certificate of Analysis not available for kit components.
    Lot Number

    Made to Order Inquiry

    Inquiry
    Host Cell Type:
    Membrane Protein Engineering:
    Fluorescent Marker:
    Resistance:
    Deliverable:

    Product Information

    Target Protein
    EDNRB
    Target Family
    Endothelin Family
    Target Protein Species
    Human
    Host Cell Type
    MDA-MB-231;BT549;CHO-K1;HEK293
    Target Classification
    GPCR Cell Lines
    Target Research Area
    Digestive and Renal Research;CNS Research
    Related Diseases
    Waardenburg Syndrome, Type 4A;Abcd Syndrome
    Gene ID
    Human: 1910
    UniProt ID
    Human: P24530

    Product Properties

    Biosafety Level
    Level 1
    Activity
    Yes
    Quantity
    10⁶ cells per vial
    Applications
    EDNRB is another critical receptor in the endothelin system. It has been associated with Hirschsprung-associated enterocolitis, where certain bacterial strains can activate specific signaling pathways in EDNRB-deficient models. Moreover, EDNRB mutations have been linked to Hirschsprung disease, a congenital disorder affecting the colon. Recent genetic studies have also identified novel variants in the EDNRB gene associated with Waardenburg syndrome, a genetic condition causing hearing loss and changes in pigmentation.

    Protocols

    Please visit our protocols page.

    Customer Reviews

    There are currently no Customer reviews or questions for mProX™ Human EDNRB Stable Cell Line (S01YF-0923-PY65). Click the button above to contact us or submit your feedback about this product.

    FAQ

    chat Gary (Verified Customer)

    How does EDNRB contribute to developmental research? Sep 12 2021

    chat Patrick Liam (Creative Biolabs Scientific Support)

    EDNRB, or endothelin receptor type B, has been studied for its role in developmental disorders, particularly Hirschsprung disease. Mutations in the EDNRB gene can lead to defects in enteric neuron development, resulting in gastrointestinal dysfunction. Understanding the role of EDNRB in development can provide insights into congenital disorders and potential therapeutic interventions. Sep 12 2021

    chat David (Verified Customer)

    What is the significance of EDNRB in vascular remodeling? May 11 2023

    chat Patrick Liam (Creative Biolabs Scientific Support)

    EDNRB, in conjunction with EDNRA, has been implicated in pathological vascular remodeling. Agents like andrographolide that modulate the endothelin signaling pathway have shown promise in regulating vascular remodeling by influencing the expression of both EDNRA and EDNRB. This suggests a coordinated role for these receptors in vascular health and disease. May 11 2023

    Published Data

    Fig.1 EDNRB silencing attenuates the malignant behaviors of TNBC cells.

    Cell viability in MDA-MB-231/EDNRBsh, control MDA-MB-231/NC, BT549/EDNRBsh, and control BT549/NC cell lines was assessed via the CCK-8 assay method.

    Ref: Gu, Xi, et al. "Knockdown of endothelin receptor B inhibits the progression of triple-negative breast cancer." Annals of the New York Academy of Sciences 1448.1 (2019): 5-18.

    Pubmed: 30900271

    DOI: 10.1111/nyas.14039

    Research Highlights

    Yang Q, et al. "mRNA sequencing provides new insights into the pathogenesis of Hirschsprung's ." Pediatric surgery international, 2023.
    The aim of the study was to identify the main susceptibility genes linked to Hirschsprung disease using RNA sequencing and RT-qPCR on colonic tissues of EDNRB(m1yzcm) and wild mice. RNA was extracted, sequencing was performed, and the obtained data were compared to the reference genome. Gene expression analysis and validation were conducted, and enrichment analyses were performed. A total of 8354 differentially expressed genes were identified, with good correlation between transcriptome and RT-qPCR data. GO and KEGG analyses revealed 8103 terms and 320 pathways, indicating a potential connection between axon guidance and focal adhesion pathways and HSCR. These findings contribute to further research on the underlying genetic causes of Hirschsprung's disease.
    Pubmed: 37676292   DOI: 10.1007/s00383-023-05544-5

    Hounye AH, et al. "Evaluation of drug sensitivity, immunological characteristics, and prognosis in ." Journal of molecular medicine (Berlin, Germany), 2023.
    Melanoma is a highly malignant cutaneous tumor with a high fatality rate and a grim prognosis. When utilizing models with multiple features, the utility of the model should be evaluated. Through the implementation of a machine learning algorithm, a signature associated with Endoplasmic Reticulum (ER) stress was developed using data from the TCGA and GEO databases. This ER stress-associated signature demonstrates a robust capacity for predicting the prognosis of melanoma.
    Pubmed: 37653150   DOI: 10.1007/s00109-023-02365-w

    Please note: All products are "FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR CLINICAL PROCEDURES" For licensing inquiries, please contact
    Send Inquiry Send Inquiry
    Inquiry Basket
    compare

    Go to compare