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  • mProX™ Human OXTR Stable Cell Line

    [CAT#: S01YF-1023-PY320]
    Product Category:
    Membrane Protein Stable Cell Lines
    Subcategory:

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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-KX987 Magic™ Rat OXTR in Vitro Calcium Flux Assay Rat CHO-K1 Calcium Flux Assay
    S01YF-1122-KX988 Magic™ Rat OXTR in Vitro IP1 Assay Rat CHO-K1 IP1 Assay

    Product Information

    Target Family
    Oxytocin Family
    Target Protein Species
    Human
    Host Cell Type
    HEK293;CHO-K1;U87MG
    Target Classification
    Other Targets Drug Discovery Assays and Products
    Target Research Area
    CNS Research;Cardiovascular Research
    Related Diseases
    Rippling Muscle Disease 2;Long Qt Syndrome 9
    Gene ID
    Human:5021
    UniProt ID
    Human:P30559

    Product Properties

    Biosafety Level
    Level 1
    Activity
    Yes
    Quantity
    10⁶ cells per vial
    Applications
    The Oxytocin receptor (OXTR) plays a pivotal role in social behavior, emotional regulation, and reproductive behaviors. It's the primary receptor for oxytocin, a neuropeptide that's been dubbed the "love hormone." Research has shown that variations in the OXTR gene can influence social recognition skills, empathy, and bonding. Moreover, dysregulation of OXTR signaling has been linked to various psychiatric disorders, including autism spectrum disorder and depression. Understanding the molecular mechanisms of OXTR can provide insights into the development of novel therapeutic strategies for these disorders.

    Protocols

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    FAQ

    chat Donna (Verified Customer)

    What are the roles of the Oxytocin Receptor (OXTR) in human diseases? Sep 24 2020

    chat Patrick Liam (Creative Biolabs Scientific Support)

    The oxytocin receptor (OXTR) is responsible for signal transduction after binding its ligand, oxytocin. Dysfunctions in OXTR and polymorphisms in the OXTR gene have been linked to the development of various diseases, highlighting its significance in human health. Sep 24 2020

    chat Amy (Verified Customer)

    Are there any associations between OXTR polymorphisms and behavioral functioning in children and adolescents? Sep 11 2023

    chat Patrick Liam (Creative Biolabs Scientific Support)

    Yes, polymorphisms in the Oxytocin receptor gene (OXTR) have been linked to various aspects of social, emotional, and behavioral functioning in children and adolescents. Notably, associations with Autism Spectrum Disorder (ASD) and conduct disorder have been observed. Sep 11 2023

    Published Data

    Fig.1 The impact of oxytocin receptor (OXTR) knockdown on cell viability, apoptosis, and cell death has been assessed, with a focus on the alteration of these cellular processes.

    The effects of oxytocin receptor (OXTR) knockdown on cell viability, apoptosis, and cell death were examined. U-87MG and U-87MG KD cells were stained with an apoptosis marker (Annexin V) and a necrosis marker (7-AAD). The viable/non-viable ratio of the cells was analyzed by a flow cytometer (n=4-6). Statistical comparisons were made using Student's t-test. Significantly different values were marked with **p<0.05 and ***p<0.001.

    Ref: Alanazi, Mohammed M., et al. "Cell proliferation and anti-oxidant effects of oxytocin and oxytocin receptors: role of extracellular signal-regulating kinase in astrocyte-like cells." Endocrine Regulations 54.3 (2020): 172-182.

    Pubmed: 32857718

    DOI: 10.2478/enr-2020-0020

    Research Highlights

    Paola Cerrito, Jeffrey K Spear "Lack of evidence for coevolution between oxytocin receptor N-terminal variants and monogamy in placental mammals." Hormones and behavior, 2023
    Oxytocin (OXT) is a neurohypophyseal hormone that plays a crucial role in the regulation of affiliative behaviors, such as pair-bonding and infant care, in mammals. The effectiveness of OXT is largely dependent on its interaction with its receptor, OXTR, which is a member of the G-protein coupled receptor family. The extracellular N-terminal domain of OXTR is responsible for binding with the C-terminal tail of OXT. Interestingly, there is a significant genetic diversity in the terminal sequence of OXTR across mammalian species. Previous studies on primates have shown a correlation between OXTR phylogeny and the evolution of monogamy. However, it remains unclear if this variation co-evolved with specific mating systems or infant care behaviors. To address this question, a phylogenetic comparative and evolutionary modeling approach was applied to a diverse group of placental mammals (n = 60). The results indicate that the diversity in the N-terminal region of OXTR is not likely to be the genetic basis for the variation in affiliative behaviors as no evidence of co-evolution between protein sequence and these behaviors was found. Therefore, it is unlikely that the impact of OXT on affiliative behaviors is influenced by the genetic diversity of its receptor.
    Paola Cerrito, Jeffrey K Spear "Lack of evidence for coevolution between oxytocin receptor N-terminal variants and monogamy in placental mammals." Hormones and behavior, 2023
    Pubmed: 37806189   DOI: 10.1016/j.yhbeh.2023.105437

    Alexey Kuznetsov et al. "Genetic Contributors to PTSD: the Role of SNVs, Gene Interactions and Haplotypes for Developing PTSD Prevention Measures. A Comprehensive Review." Psychiatria Danubina, 2023
    In this study, an examination was conducted on post-traumatic stress disorder (PTSD), a mental health condition associated with high socioeconomic burden. The authors aimed to identify potential genetic markers that may predispose individuals to PTSD, with the goal of informing future research on developing preventative and remedial measures. The study involved a literature review of 547 articles from the PubMed database, of which 20 met the inclusion criteria. Results showed significant associations between PTSD and various genetic variants, such as FKBP5 rs9470080, two FKBP5 haplotypes, and certain gene-gene interactions. However, our current understanding of the complex genetic factors involved in PTSD remains limited, and further exploration of epigenetic mechanisms is needed. Future research should prioritize examining these aspects to gain a more comprehensive understanding of the disorder and its underlying genetics.
    Alexey Kuznetsov et al. "Genetic Contributors to PTSD: the Role of SNVs, Gene Interactions and Haplotypes for Developing PTSD Prevention Measures. A Comprehensive Review." Psychiatria Danubina, 2023
    Pubmed: 37800217   DOI: No

    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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