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  • mProX™ Human DRD3 Stable Cell Line

    [CAT#: S01YF-0923-PY61]
    Product Category:
    Membrane Protein Stable Cell Lines
    Subcategory:
    GPCR Cell Lines

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    Product Information

    Target Protein
    DRD3
    Target Family
    Dopamine Family
    Target Protein Species
    Human
    Host Cell Type
    HeLa;CHO-K1;HEK293
    Target Classification
    GPCR Cell Lines
    Target Research Area
    CNS Research
    Related Diseases
    Tremor, Hereditary Essential, 1;Schizophrenia
    Gene ID
    Human: 1814
    UniProt ID
    Human: P35462

    Product Properties

    Biosafety Level
    Level 1
    Activity
    Yes
    Quantity
    10⁶ cells per vial
    Applications
    The Dopamine Receptor D3 (DRD3) has been a focal point in various scientific research endeavors. It plays a pivotal role in the dopamine system, which is integral to many neurological processes. Studies have shown that DRD3 is associated with several neuropsychiatric disorders, including schizophrenia. Moreover, its polymorphisms have been linked to the efficacy of antipsychotic treatments. This receptor's significance is further underscored by research into its potential as a therapeutic target for Parkinson's disease. The intricacies of DRD3's function and its implications in neuropsychiatric conditions make it a compelling subject for ongoing research.

    Protocols

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    FAQ

    chat Dorothy (Verified Customer)

    What are the benefits of using a stable cell line for rAAV production? Sep 24 2021

    chat Patrick Liam (Creative Biolabs Scientific Support)

    Stable cell lines offer a time-efficient and robust process for rAAV production, addressing manufacturing challenges for rAAV-based medicines. Sep 24 2021

    chat Joseph (Verified Customer)

    How can stable cell lines assist in studying RAGE-targeting molecules? Oct 30 2021

    chat Patrick Liam (Creative Biolabs Scientific Support)

    Stable cell lines, such as the hRAGE-NIH3T3 cell line, serve as excellent tools for studying RAGE-targeting molecules based on cellular level, biological function, and Rage-mediated molecular mechanisms. Oct 30 2021

    Published Data

    Fig.1 DRD3 serves as the intermediary for the actions induced by Prazosin.

    The subcellular distribution of DRD3 was assessed in GFP-DRD3-FLAG-HeLa cells. These cells were exposed to either control DMSO or 30 μM Prazosin for an hour, followed by fixation in PBS + formaldehyde. Subsequently, anti-GFP antibody staining was performed under two conditions: one with 0.1% Triton X-100 permeabilization (left), and the other without permeabilization (right). Remarkably, live GFP-DRD3-FLAG-HeLa cells exhibited congruent localization patterns with permeabilized cells, suggesting that the membrane-bound DRD3 population is comparatively sparse in contrast to its intracellular counterpart, akin to transferrin receptor. Notably, a commercially available anti-DRD3 antibody exhibited substantial non-specific staining and was unsuitable for immunofluorescence. (Scale bar: 10 μm.)

    Ref: Zhang, Xin, et al. "Dopamine receptor D3 regulates endocytic sorting by a Prazosin-sensitive interaction with the coatomer COPI." Proceedings of the National Academy of Sciences 109.31 (2012): 12485-12490.

    Pubmed: 22802617

    DOI: 10.1073/pnas.1207821109

    Research Highlights

    Salminen SP, et al. "Genetic risk scores associated with temperament clusters in Finnish depression ." Acta neuropsychiatrica, 2023.
    Cloninger's temperament dimensions have been extensively studied in relation to genetics. The present study examined the associations between Cloninger's temperament dimensions and single nucleotide polymorphisms (SNPs) through cluster analyses. It involved 212 genotyped Finnish patients from the Ostrobothnia Depression Study. Selected depression-related genes were analyzed, and a total of 59 SNPs from ten genes were investigated. No significant associations were found between individual SNPs and temperament clusters. However, multivariate models and genetic risk score (GRS) analyses revealed significant associations between GRSs and temperament clusters, with two SNPs from the DRD3, SLC6A2, SLC6A4, and HTR2A genes associated with the HHA/LRD/LP cluster at baseline and six weeks, and the HTR2A and COMT genes associated with the HP cluster at six weeks. These findings suggest that GRSs may be linked to an individual's temperament profile, and further research is needed to investigate the clinical implications of these clusters.
    Pubmed: 37665031   DOI: 10.1017/neu.2023.33

    Fitzgerald E, et al. "Sex and cell-specific gene expression in corticolimbic brain regions associated ." EBioMedicine, 2023.
    The study reveals significant sex-specific differences in the prevalence, symptomatology, and course of psychiatric disorders. However, preclinical models have typically focused on male subjects, resulting in a limited understanding of the molecular mechanisms driving these differences. The authors conduct transcriptome-wide gene expression analysis in male and female rats within the corticolimbic system, identifying over 3000 differentially expressed genes (DEGs) in the nucleus accumbens medial shell (NAcS). Further analysis shows that these DEGs are enriched for gene ontology terms related to blood vessel morphogenesis and cell migration. Additionally, single nuclei RNA sequencing in the NAcS identifies widespread sex-specific expression, with upregulated genes in females enriched for synaptic function. Notably, these upregulated genes are also linked to psychiatric disorders in humans. These findings highlight the importance of considering sex- and cell-specific molecular profiles in understanding psychiatric disorders, particularly in the NAcS region. This study was supported by funding from the Hope for Depression Research Foundation (MJM).
    Pubmed: 37549631   DOI: 10.1016/j.ebiom.2023.104749

    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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