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  • mProX™ Human DRD4 Stable Cell Line

    [CAT#: S01YF-0923-PY62]
    Product Category:
    Membrane Protein Stable Cell Lines
    Subcategory:
    GPCR Cell Lines

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    Based on this stable cell line, we also provide cell-based in vitro assays to evaluate the effects of your compounds or antibodies.

    Sub Cat Product Name Target Protein Species Host Cell Type Assay Types Inquiry Datasheet
    S01YF-1122-KX413 Magic™ Rat DRD4 in Vitro [35S]GTPγS binding Assay Rat CHO-K1 [35S]GTPγS binding Assay
    S01YF-1122-KX414 Magic™ Rat DRD4 in Vitro Radioligand Binding Assay Rat CHO-K1 Radioligand Binding Assay

    Product Information

    Target Protein
    DRD4
    Target Family
    Dopamine Family
    Target Protein Species
    Mouse
    Host Cell Type
    RAW;264.7;CHO-K1;HEK293
    Target Classification
    GPCR Cell Lines
    Target Research Area
    CNS Research
    Related Diseases
    Attention Deficit-Hyperactivity Disorder;Autonomic Nervous System Disease
    Gene ID
    Mouse: 13491
    UniProt ID
    Mouse: P51436

    Product Properties

    Biosafety Level
    Level 1
    Activity
    Yes
    Quantity
    10⁶ cells per vial
    Applications
    The Dopamine Receptor D4 (DRD4) has garnered attention in the realm of scientific research due to its association with various behavioral and neurological conditions. One study highlighted its role in antisaccade performance, suggesting two modes of antisaccade processing influenced by the DRD4 genotype. Furthermore, research has linked specific combinations of variants in the DRD4 gene with eating disorders, emphasizing its potential role in psychopathological features. Additionally, DRD4 has been implicated in the regulation of functional integration of brain networks in children with ADHD. The multifaceted implications of DRD4 in health and disease make it a crucial subject in scientific investigations.

    Protocols

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    FAQ

    chat Joseph (Verified Customer)

    What is the significance of DRD4 in scientific research? Feb 11 2022

    chat Patrick Liam (Creative Biolabs Scientific Support)

    DRD4, also known as the dopamine receptor D4, plays a pivotal role in various neurological and psychological processes. It has been extensively studied for its association with attention-deficit hyperactivity disorder (ADHD) and its potential influence on novelty-seeking behavior. The receptor's polymorphisms, especially the variable number tandem repeats (VNTRs) in the third exon, have been linked to differences in human behavior and susceptibility to certain psychiatric disorders. Moreover, DRD4 has been implicated in the modulation of synaptic plasticity and cognition, making it a focal point in neuroscientific research. Feb 11 2022

    chat Sandra (Verified Customer)

    How does DRD4 contribute to our understanding of neuropsychiatric disorders? Mar 13 2023

    chat Patrick Liam (Creative Biolabs Scientific Support)

    The genetic variations in DRD4, particularly the 7-repeat allele of the VNTR, have been associated with ADHD, making it a potential therapeutic target1. Furthermore, its involvement in the dopamine pathway suggests its role in reward and motivation systems of the brain. Understanding the function and regulation of DRD4 can provide insights into the neurochemical basis of behavior and offer avenues for targeted treatments in neuropsychiatric conditions. Mar 13 2023

    Published Data

    Fig.1 Upon DRD4 silencing using siRNA, the impact of dopamine (DA) on IL-1β and TNF-α within tumor-associated macrophages (TAMs) was notably attenuated.

    Subsequent to the suppression of DRD4, the impact of dopamine (DA) on IL-1β and TNF-α was attenuated within tumor-associated macrophages (TAMs) derived from bone marrow, as discerned through RT-PCR analysis.

    Ref: Liu, Qiaofei, et al. "Dopamine improves chemotherapeutic efficacy for pancreatic cancer by regulating macrophage-derived inflammations." Cancer Immunology, Immunotherapy 70 (2021): 2165-2177.

    Pubmed: 33454798

    DOI: 10.1007/s00262-020-02816-0

    Research Highlights

    Mostafalou S, Abdollahi M. "The susceptibility of humans to neurodegenerative and neurodevelopmental ." Archives of toxicology, 2023.
    The field of toxicology investigates the effects of organophosphorus (OP) compounds on human health. These substances have been linked to an increased likelihood of neurological disorders, such as neurodegenerative and neurodevelopmental diseases. This review examines various studies on the role of OP compounds in the development of these disorders and explores how genetic variations can impact susceptibility to their neurotoxic effects. Research has shown that exposure to OP compounds can lead to the development of conditions like Alzheimer's disease, Parkinson's disease, attention deficit hyperactivity disorder, autism, intellectual disability, and other developmental neurotoxicities. In addition to inhibiting the cholinesterase enzyme, it is believed that OP compounds contribute to these disorders through other pathological mechanisms at both the extracellular and intracellular levels. Certain genetic polymorphisms, including PON1, ABCB1, NOS, DRD4, GST, CYP, and APOE, have been linked to an increased risk of developing OP-related neurological disorders.
    Pubmed: 37787774   DOI: 10.1007/s00204-023-03604-2

    Estandia A, et al. "Candidate gene polymorphisms are linked to dispersive and migratory behaviour: ." Journal of evolutionary biology, 2023.
    In a study of partial migrant populations, research found that individuals who migrated typically displayed longer microsatellite alleles at the CLOCK gene compared to resident individuals within the same group. Further analysis revealed that populations which had been recently colonized (within 200 years) showed longer average microsatellite allele lengths at CREB1, compared to populations with a longer evolutionary history. However, Bayesian broken stick regression models demonstrated a decrease in CREB1 length over time since colonization. Similar patterns were observed for DRD4, although a larger sample size is needed for confirmation. While genes ADCYAP1, SERT, and NPAS2 showed variability, this was not linked to dispersal behavior. These findings suggest a potential link between genetic variants at these specific genes and the ability for migration and dispersal in silvereyes, and highlight the need for further investigation into the genetic mechanisms underlying these behaviors. It also presents an opportunity to solve an evolutionary paradox using a genetic approach.
    Pubmed: 37750610   DOI: 10.1111/jeb.14222

    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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