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  • mProX™ Human TRHR Stable Cell Line

    [CAT#: S01YF-0923-KX53]
    Product Category:
    Membrane Protein Stable Cell Lines
    Subcategory:
    GPCR Cell Lines

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    Product Information

    Target Protein
    TRHR
    Target Family
    TRH Family
    Target Protein Species
    Human
    Host Cell Type
    CHO-K1; HEK293
    Target Classification
    GPCR Cell Lines
    Target Research Area
    Reproductive Research
    Related Diseases
    Hypothyroidism; Congenital; Nongoitrous; Hypothyroidism
    Gene ID
    UniProt ID

    Product Properties

    Biosafety Level
    Level 1
    Activity
    Yes
    Quantity
    10⁶ cells per vial
    Applications
    The rhodopsin-like receptor family's group A7 includes the seven transmembrane domain GTP (G) protein coupled receptors (GPCRs) known as TRH receptors (TRHRs). Rodents have been the subject of extensive research on TRHR, leading to the identification of two variants, TRHR1 and TRHR2. TRHR is essential for several biological processes, including fending off depression, lowering anxiety, and enhancing learning and memory. Numerous studies show a connection between TRHR and a number of illnesses, including diabetes, breast cancer, depression, spinal cord injury, and amyotrophic lateral sclerosis. Clinical therapy may benefit from controlling TRH synthesis in the hypothalamus and patterns of TRH and its receptor expression throughout the body. The customized TRHR stable cell line can be used in antibody discovery and development, potential drug candidate screening and signaling pathway researches.

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    Published Data

    Fig.1 The production of a punctate vesicular location of -arrestin 1-GFP is dependent on effective internalization of the TRHR-1 truncation mutants.

    Either mock transfected or -arrestin 1-GFP (green)-expressing HEK293 cells were used. The cells were given a vehicle or TRH (1 M, 60 min) treatment before being fixed without permeabilization and labeled with an anti-VSV monoclonal antibody and a secondary antiserum that was Alexa 594-labeled (red).

    Ref: Groarke, D. Alex, et al. "Analysis of the C-terminal tail of the rat thyrotropin-releasing hormone receptor-1 in interactions and cointernalization with β-arrestin 1-green fluorescent protein." Molecular Pharmacology 59.2 (2001): 375-385.

    Pubmed: 11160875

    DOI: 10.1124/mol.59.2.375

    Research Highlights

    An original mistake With central hypothyroidism in homozygotes and hyperthyrotropinemia in heterozygotes, the TRHR deficiency seen in a consanguineous family suggests compensatory increase of TSH with diminished biopotency.
    García, Marta, et al. "Central hypothyroidism due to a TRHR mutation causing impaired ligand affinity and transactivation of Gq." The Journal of Clinical Endocrinology & Metabolism 102.7 (2017): 2433-2442.
    Pubmed: 28419241   DOI: 10.1210/jc.2016-3977

    Peng, Xiao, Tiejian Li, and John D. Albertson. "Investigating predictability of the TRHR seasonal precipitation at long lead times using a generalized regression model with regularization." Frontiers in Earth Science 9 (2021): 724599.
     

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