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  • mProX™ Human OPRL1 Stable Cell Line

    [CAT#: S01YF-0923-PY154]
    Product Category:
    Membrane Protein Stable Cell Lines
    Subcategory:
    GPCR Cell Lines

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    Product Information

    Target Protein
    OPRL1
    Target Family
    Opioid Family
    Target Protein Species
    Human
    Host Cell Type
    PANC1;MiaPaCa2;CHO-K1;HEK293
    Target Classification
    GPCR Cell Lines
    Target Research Area
    Pain and Addiction Research;CNS Research
    Related Diseases
    Drug Dependence;Anxiety
    Gene ID
    Human: 4987
    UniProt ID
    Human: P41146

    Product Properties

    Biosafety Level
    Level 1
    Activity
    Yes
    Quantity
    10⁶ cells per vial
    Applications
    The OPRL1 gene encodes the nociceptin receptor, which is involved in various physiological and pathological processes. Recent studies have highlighted the epigenetic regulation of OPRL1 in the context of adverse maternal environments, suggesting its potential role in neurocognitive impairment in offspring. Furthermore, elevated methylation of OPRL1 has been observed in Alzheimer's disease, indicating its potential as a methylation biomarker for diagnosis. Another study has shown that curcumin can downregulate the expression of OPRL1 in isolated neuroglia cells, which is associated with pain relief. Additionally, methylation of OPRL1 has been linked to the effects of psychosocial stress on binge drinking in adolescents, providing insights into the epigenetic mechanisms underlying substance abuse.

    Protocols

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    FAQ

    chat Amy (Verified Customer)

    How does the adverse maternal environment impact the expression of OPRL1 in the hippocampus? Sep 01 2022

    chat Patrick Liam (Creative Biolabs Scientific Support)

    An adverse maternal environment and a Western diet can contribute to neurocognitive impairment in male offspring through the epigenetic regulation of OPRL1, affecting its variant-specific and sex-specific expression in the hippocampus. Sep 01 2022

    chat Robert (Verified Customer)

    Is there a connection between OPRL1 methylation and Alzheimer's disease? Jul 06 2022

    chat Patrick Liam (Creative Biolabs Scientific Support)

    Yes, elevated methylation of the OPRL1 gene has been suggested as a potential biomarker for the diagnosis of Alzheimer's disease, indicating a role of opioid receptor genes in the disease's development. Jul 06 2022

    Published Data

    Fig.1 OPRL1 is not required for JTC801-induced alkaliptosis.

    Silencing OPRL1 through shRNA in cells exhibiting elevated OPRL1 levels failed to inhibit JTC801-triggered alkaliptosis. The reduction of OPRL1 had no impact on JTC801-induced cell death (10 µM, 24 hours) in PANC1 and MiaPaCa2 cells, as confirmed by three independent experiments (n=3, n.s=not significant).

    Ref: Song, Xinxin, et al. "JTC801 induces pH-dependent death specifically in cancer cells and slows growth of tumors in mice." Gastroenterology 154.5 (2018): 1480-1493.

    Pubmed: 29248440

    DOI: 10.1053/j.gastro.2017.12.004

    Research Highlights

    Xiaoqin Z, et al. "Development of a prognostic signature for immune-associated genes in bladder ." International urology and nephrology, 2023.
    Bladder cancer predominantly affects men and is a common malignancy of the urinary system. Although surgery alone is typically the main treatment option, platinum-based chemotherapy has shown some improvements in overall survival. However, conventional chemotherapy can come with unpleasant side effects, prompting researchers to explore alternative therapies such as immunotherapy. In this study, the authors utilized bioinformatics analyses on The Cancer Genome Atlas (TCGA) database to develop an immune-associated prognostic signature for bladder cancer. This signature included 1 LncRNA (NR2F1-AS1) and 16 mRNAs, which were used to predict a potential therapeutic drug through the Connectivity Map database. The drug, Cephaeline, was found to effectively inhibit the growth of T24 bladder cancer cells. Ultimately, this new predictive pattern enables more targeted and effective treatment for bladder cancer patients and lays the groundwork for future immunotherapy trials in this field.
    Pubmed: 37740848   DOI: 10.1007/s11255-023-03796-7

    Hu R, et al. "Selection signature analysis reveals RDH5 performed key function in vision during ." Archives animal breeding, 2023.
    In the Neolithic age, sheep were one of the most successful domesticated animals and gradually spread across the world through human activities. The domestication process resulted in changes in the sheep's morphology, physiology, and behavior, leading to the emergence of different breeds with unique characteristics through artificial and natural selection. However, the underlying genetic basis responsible for these variations remains largely unidentified. This study utilized whole genome resequencing technology to compare and analyze the genome differences between Asiatic mouflon wild sheep (Ovis orientalis) and Hu sheep (Ovis aries). Through this analysis, 755 genes were identified to have undergone positive selection during the domestication and selection process. Of interest were the genes related to sensory perception that displayed directional evolution in the autosomal region, including OPRL1, LEF1, TAS1R3, ATF6, VSX2, MYO1A, RDH5, and several novel genes. A missense mutation, c.T722C/p.M241T, was discovered in exon 4 of RDH5 in sheep, and the T allele was completely fixed in Hu sheep. Furthermore, the mutation with the C allele resulted in reduced retinol dehydrogenase activity encoded by RDH5, affecting retinoic acid metabolism and influencing the visual cycle. In conclusion, this study demonstrated that during sheep domestication, there was a significant enrichment for positively selected genes involved in sensory perception development. Additionally, the missense mutation in RDH5 and its variants may be associated with retinal degeneration in sheep. It is hypothesized that humans eliminated wild sheep ancestors with weaker visual sensitivity, and the mutation was selectively favored under the dual pressures of natural and artificial selection.
    Pubmed: 37384328   DOI: 10.5194/aab-66-81-2023

    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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