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  • mProX™ Human GPR45 Stable Cell Line

    [CAT#: S01YF-0923-PY192]
    Product Category:
    Membrane Protein Stable Cell Lines
    Subcategory:
    GPCR Cell Lines

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    Product Information

    Target Protein
    GPR45
    Target Family
    Orphan Family
    Target Protein Species
    Mouse
    Host Cell Type
    Primary hypothalamic cells;CHO-K1;HEK293
    Target Classification
    GPCR Cell Lines
    Target Research Area
    Digestive and Renal Research;Cardiovascular Research
    Related Diseases
    Diversion Colitis;Vascular Parkinsonism
    Gene ID
    Mouse: 93690
    UniProt ID
    Mouse: Q9EQQ4

    Product Properties

    Biosafety Level
    Level 1
    Activity
    Yes
    Quantity
    10⁶ cells per vial
    Applications
    GPR45, another member of the G protein-coupled receptor family, has been less extensively studied compared to other GPCRs. However, preliminary research indicates its potential involvement in metabolic processes and immune system modulation. As with many GPCRs, the exact physiological roles and potential therapeutic applications of GPR45 remain to be fully elucidated. Continued research in this area is anticipated to shed light on its function and relevance in health and disease.

    Protocols

    Please visit our protocols page.

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    There are currently no Customer reviews or questions for mProX™ Human GPR45 Stable Cell Line (S01YF-0923-PY192). Click the button above to contact us or submit your feedback about this product.

    FAQ

    chat Linda (Verified Customer)

    What is the primary function of GPR45 in the body? Feb 23 2021

    chat Patrick Liam (Creative Biolabs Scientific Support)

    GPR45, also known as GPR45, is a G-protein coupled receptor that plays a role in various physiological processes. Its specific functions and ligands are still under investigation. Feb 23 2021

    chat Shirley (Verified Customer)

    Are there any known diseases or conditions associated with GPR45? Aug 22 2020

    chat Patrick Liam (Creative Biolabs Scientific Support)

    Current research is exploring the potential associations between GPR45 and various diseases. However, definitive links are yet to be established. Aug 22 2020

    Published Data

    Fig.1 Gpr45 knockdown in primary hypothalamus cells resulted in Pomc downregulation.

    In primary hypothalamic cells, the suppression of Gpr45 led to a notable decrease in Pomc expression levels. The results are presented as the mean ± SEM, with statistical significance indicated by asterisks (*P < 0.05, **P < 0.01, and ***P < 0.001) as determined through Student's t-test analysis.

    Ref: Cui, Jing, et al. "Disruption of Gpr45 causes reduced hypothalamic POMC expression and obesity." The Journal of clinical investigation 126.9 (2016): 3192-3206.

    Pubmed: 27500489

    DOI: 10.1172/JCI85676

    Research Highlights

    Tsai MC, et al. "Genome-wide association study of age at menarche in the Taiwan Biobank suggests ." Journal of human genetics, 2023.
    The process of sexual maturation is an intricate physiological process that is influenced by various factors, including genetic and environmental elements. In females, the age at which they experience their first menstruation, also known as menarche (AM), is a crucial milestone in sexual maturation. This study, utilizing data from a national population cohort in Taiwan, aimed to identify genetic markers associated with AM. Through a genome-wide association study and meta-analysis, four significant loci - LIN28B, NOL4, GPR45, and LOC105373831 - were found to be linked with AM. Further analyses also revealed LIN28B, NOL4, RXRG, ETV5, and HACE1 as significantly associated genes, while a specific genetic pathway involving the mTOR signaling complex showed enrichment. The study also identified a new genetic marker, rs7239368 in NOL4, that was associated with AM in the Taiwanese female population. Further research is needed to validate its role in sexual maturation.
    Pubmed: 36710296   DOI: 10.1038/s10038-023-01124-6

    Tsai MC, et al. "Identification of genetic risk loci for depression and migraine comorbidity in ." Frontiers in psychiatry, 2022.
    The genetic association between depression and migraine in Asian populations has not been extensively studied. The underlying genetic factors for comorbid depression and different types of migraine remain unclear. Therefore, a study was conducted in Taiwan to investigate susceptibility loci associated with depression and migraine comorbidity in the Han Chinese population. The study involved 966 participants with migraine, with or without depression, and genotyping was performed using their genomic DNA. Results suggest that several genetic variants, including CDH4 intron region (rs78063755), NTRK3-AS1 downstream region (rs57729223), and between LINC01918 and GPR45 (rs2679891), may be suggestive of an association with depression. Additionally, 20 more susceptibility loci were identified within specific subgroups of migraine. Furthermore, a specific variant in the CDH4 intron region (rs78063755) was found to be associated with both Beck Depression Inventory and Migraine Disability Assessment scores. These findings provide potential genetic candidates for further research on the genetic basis of depression and migraine comorbidity in the Han Chinese population.
    Pubmed: 36704746   DOI: 10.3389/fpsyt.2022.1067503

    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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