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  • mProX™ Human ADRB3 Stable Cell Line

    [CAT#: S01YF-0923-PY13]
    Product Category:
    Membrane Protein Stable Cell Lines
    Subcategory:
    GPCR Cell Lines

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    Product Information

    Target Protein
    ADRB3
    Target Family
    Adrenergic Family
    Target Protein Species
    Mouse
    Host Cell Type
    MSCs;CHO-K1;HEK293
    Target Classification
    GPCR Cell Lines
    Target Research Area
    CNS Research
    Related Diseases
    Body Mass Index Quantitative Trait Locus 11;Leptin Deficiency Or Dysfunction
    Gene ID
    Mouse: 11556
    UniProt ID
    Mouse: P25962

    Product Properties

    Biosafety Level
    Level 1
    Activity
    Yes
    Quantity
    10⁶ cells per vial
    Applications
    The ADRB3 gene, encoding the beta-3 adrenergic receptor, has garnered attention in the scientific community for its diverse roles in physiological processes. This receptor is predominantly expressed in brown adipose tissue and is involved in the regulation of lipolysis and thermogenesis. Recent research has unveiled the endocrine role of brown adipose tissue (BAT) in cardiac remodeling, where the activation of ADRB3 in brown adipocytes offers cardioprotection by suppressing exosomal iNOS. Moreover, the ADRB3 gene has been associated with overactive bladder syndrome, with studies suggesting that alterations in serum ROCK2 levels combined with ADRB3 levels can provide insights into the pathophysiology of the condition. Additionally, the ADRB3 gene has been implicated in the progression of heart failure, where the crosstalk between HDAC3, microRNA-18a, and ADRB3 plays a pivotal role. In essence, the ADRB3 gene has a broad spectrum of applications in scientific research, ranging from cardiovascular health to urinary disorders and metabolic regulation.

    Protocols

    Please visit our protocols page.

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    FAQ

    chat Elizabeth (Verified Customer)

    Does ADRB3 activation in brown adipocytes have any effect on cardiac protection? May 11 2023

    chat Patrick Liam (Creative Biolabs Scientific Support)

    Yes, activation of ADRB3 in brown adipocytes offers cardiac protection by suppressing exosomal iNOS. May 11 2023

    chat Kevin (Verified Customer)

    Is there a relationship between ADRB3 gene methylation and obesity? Jun 02 2023

    chat Patrick Liam (Creative Biolabs Scientific Support)

    Epigenetic changes in the ADRB3 gene locus may be linked to the development of obesity and diseases associated with trans-fat intake and altered lipid profiles. Jun 02 2023

    Published Data

    Fig.1 In vitro effects on NE to MSC osteogenic differentiation

    Alizarin Red staining showed that NE-treated MSCs had markedly less ability to form mineralized nodules than control MSCs, but knockdown of the adrb3 gene using siRNA abolished the NE-induced inhibition of osteogenesis.

    Ref: Du, Zhaojie, et al. "Sympathetic denervation-induced MSC mobilization in distraction osteogenesis associates with inhibition of MSC migration and osteogenesis by norepinephrine/adrb3." PLoS One 9.8 (2014): e105976.

    Pubmed: 25144690

    DOI: 10.1371/journal.pone.0105976

    Research Highlights

    Desevin K, et al. "Adrenergic Reprogramming of Preexisting Adipogenic Trajectories Steer Naive Mural ." bioRxiv : the preprint server for biology, 2023.
    In adult white adipose tissue, thermogenic beige adipocytes are promoted by cold or beta3-adrenoceptor activation. According to a comprehensive single-cell analysis, these cells originate from the reprogramming of current adipogenic pathways rather than from a single precursor. The main source of these pathways is the vascular mural progenitor cells expressing SM22. The crucial step in this process is the activation of Adrb3 in mature adipocytes, leading to the subsequent increase of Adrb1 in progenitor cells. Under thermoneutral conditions, the activation of both Adrb3 and Adrb1 together mimics the recruitment of SM22+ cells induced by cold. Lipolysis-derived eicosanoids, namely docosahexaenoic acid (DHA) and arachidonic acid (AA), trigger these pathways and can replicate the priming of progenitor cells in vitro. Overall, these findings present a strong model for the development of beige adipocytes in response to cold, highlighting the important relationship between mature adipocytes and mural cells during this process and showcasing the metabolic potential of this distinct cellular reservoir.
    Pubmed: 37662295   DOI: 10.1101/2023.08.26.554950

    Potocka N, et al. "Effects of the Trp64Arg Polymorphism in the ADRB3 Gene on Body Composition, ." Genes, 2023.
    In this study of young, healthy adults (N=304), the authors aimed to examine the association of the ADRB3 rs4994 polymorphism with body composition, somatotype, cardiorespiratory fitness, and physical activity. The ADRB3 gene plays a role in energy expenditure through lipolysis. While previous studies have investigated the polymorphism in athletes, overweight individuals, and patients with obesity and diabetes, there has been no such research on young, healthy adults. Using a PCR-RFLP method, the researchers genotyped for the ADRB3 gene and assessed anthropometric measurements, somatotypes, cardiorespiratory fitness, and physical activity levels. In the male subgroup, the Trp64Trp genotype was associated with various body components such as waist and hip circumference, body fat percentage and mass, BMI, and ratios of waist circumference to height and hip circumference to height. The Trp64Trp genotype also showed an association with somatotype components. Conversely, the Arg allele was linked with ectomorphic components. In addition, the Trp64Trp genotype was positively correlated with maximal oxygen uptake and oxygen pulse. In the female subgroup, the Trp64Trp genotype was negatively associated with reported moderate-intensity exercise. Overall, the Trp64 allele was found to be related to anthropometric traits, somatotype, and physical performance parameters in males, while the Trp64Arg polymorphism was associated with the level of physical activity for moderate-intensity exercise in females.
    Pubmed: 37628593   DOI: 10.3390/genes14081541

    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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