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  • mProX™ Human NPY2R Stable Cell Line

    [CAT#: S01YF-0923-PY139]
    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-KX699 Magic™ Rhesus monkey NPY2R in Vitro Calcium Flux Assay Rhesus monkey CHO-K1 Calcium Flux Assay
    S01YF-1122-KX700 Magic™ Rhesus monkey NPY2R in Vitro cAMP Assay Rhesus monkey CHO-K1 cAMP Assay
    S01YF-1122-KX701 Magic™ Rhesus monkey NPY2R in Vitro Radioligand Binding Assay Rhesus monkey CHO-K1 Radioligand Binding Assay

    Product Information

    Target Protein
    NPY2R
    Target Family
    Neuropeptide Y Family
    Target Protein Species
    Mouse
    Host Cell Type
    BV-2;CHO-K1;HEK293
    Target Classification
    GPCR Cell Lines
    Target Research Area
    CNS Research;Cardiovascular Research
    Related Diseases
    Temporal Lobe Epilepsy;Peripheral Artery Disease
    Gene ID
    Mouse: 18167
    UniProt ID
    Mouse: P97295

    Product Properties

    Biosafety Level
    Level 1
    Activity
    Yes
    Quantity
    10⁶ cells per vial
    Applications
    Neuropeptide Y receptor Y2 (NPY2R) is a G-protein coupled receptor that plays a vital role in various physiological processes. In the realm of scientific research, NPY2R has been associated with the regulation of food intake, energy balance, and circadian rhythms. Furthermore, it has been implicated in the modulation of anxiety and stress responses, suggesting its potential as a therapeutic target for anxiety disorders. The receptor's involvement in the central nervous system and its interactions with other neurotransmitters make it a focal point for understanding complex neural pathways and their implications in neuropsychiatric disorders.

    Protocols

    Please visit our protocols page.

    Customer Reviews

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    FAQ

    chat Matthew (Verified Customer)

    How does NPY2R influence the progression of osteoarthritis? Sep 23 2021

    chat Patrick Liam (Creative Biolabs Scientific Support)

    NPY2R is directly involved in cartilage homeostasis. The administration of rapamycin in vitro has been shown to counteract NPY-mediated effects, exacerbating the progression of osteoarthritis. This suggests a potential therapeutic target for managing osteoarthritis progression. Sep 23 2021

    chat Michelle (Verified Customer)

    Can NPY2R be associated with obesity? Aug 18 2022

    chat Patrick Liam (Creative Biolabs Scientific Support)

    There is no significant association found between sequence variants in the NPY2R gene and early onset obesity. This suggests that NPY2R may not play a crucial role in the development of obesity, at least not as a sole or primary factor. Aug 18 2022

    Published Data

    Fig.1 NPY2R overexpression increased BV-2 cell viability, whereas NPY2R knockdown decreased it.

    Enhanced expression of NPY2R substantially bolstered the survival rates of BV-2 cells, in stark contrast to the dampened viability observed with NPY2R depletion. The CCK-8 assay effectively scrutinized how BV-2 cell viability reacted when NPY2R was either upregulated or downregulated, yielding noteworthy alterations in their survival dynamics.

    Ref: Yan, Wenhui, et al. "Neuropeptide Y in the amygdala contributes to neuropathic pain-like behaviors in rats via the neuropeptide Y receptor type 2/mitogen-activated protein kinase axis." Bioengineered 13.4 (2022): 8101-8114.

    Pubmed: 35313782

    DOI: 10.1080/21655979.2022.2051783

    Research Highlights

    Hashemi Karoii D, et al. "Altered G-Protein Transduction Protein Gene Expression in the Testis of Infertile ." DNA and cell biology, 2023.
    Recent studies have shown that various members of the G-protein-coupled receptors (GPCR) superfamily play crucial roles in maintaining ion-water homeostasis in sperm and Sertoli cells, developing germ cells, forming blood barriers, and maturing sperm. Microarray analysis and bioinformatics were used to analyze GPCR, guanyl-nucleotide exchange factor, membrane traffic protein, and small GTPase genes in 3513 sperm and Sertoli cell genes. In sperm from three cases of nonobstructive azoospermia, GOLGA8IP, OR2AT4, PHKA1, and other genes were upregulated, while MARS, SIRPG, OGFR, and others were downregulated. In Sertoli cells, GBP3, TNF, TGFB3, and CLTC expression was increased, while PAQR4, RRAGD, RAC2, and others were downregulated. An analysis of Enrich Shiny Gene Ontology (GO), STRING, and Cytoscape predicted protein interactions and identified key pathways. Functional enrichment analysis showed that DEGs were significantly expressed in biological processes, such as regulating protein metabolic processes and small GTPase-mediated signal transduction, and in molecular functions, such as GPCR activity and guanyl ribonucleotide binding. The analysis of Sertoli cells showed similar DEGs. Validating these gene mutations could lead to the development of new, receptor-selective GPCR antagonists and agonists.
    Pubmed: 37610843   DOI: 10.1089/dna.2023.0189

    Shen Y, et al. "Identification of hub genes in digestive system of mandarin fish (Siniperca ." Comparative biochemistry and physiology. Part D, Genomics & proteomics, 2023.
    Mandarin fish (Siniperca chuatsi) is a commercially important freshwater species and a carnivorous fish. The digestive system, consisting of the liver, stomach, intestine, pyloric caecum, esophagus, and gallbladder, plays a crucial role in understanding fish domestication. In a previous study, it was found that domestication of mandarin fish led to changes in the histological morphology and gene expression levels of the digestive system when exposed to artificial diet. However, the specific hub genes highly associated with this domestication process have not been identified. In this study, WGCNA was performed on 17 tissue and 9 developmental stage transcriptomes, combined with differential gene expression analysis of the digestive system, to identify key hub genes involved in the adaptation of mandarin fish to artificial diet. A total of 31,657 genes from 26 samples were classified into 23 color modules by WGCNA. The modules midnightblue, darkred, lightyellow, and darkgreen were strongly associated with the liver, stomach, esophagus, and gallbladder, respectively. The hub genes in the liver included cp, vtgc, c1in, c9, lect2, and klkb1. In the stomach, hub genes included ghrl, atp4a, gjb3, muc5ac, duox2, and chia2. Mybpc1, myl2, and tpm3 were identified as hub genes in the esophagus, while dyst, npy2r, slc13a1, and slc39a4 were hub genes in the gallbladder. The intestine and pyloric caecum were associated with hub genes slc15a1, cdhr5, btn3a1, anpep, slc34a2, cdhr2, and ace2. Additionally, pathway analysis revealed that modules related to the digestive system were mainly enriched in digestion and absorption, metabolism, and immune-related pathways. Furthermore, after domestication, the hub genes vtgc and lect2 were significantly upregulated in the liver, chia2 was significantly downregulated in the stomach, and slc15a1, anpep, and slc34a2 were significantly upregulated in the intestine. This study presents a comprehensive analysis of the hub genes associated with the adaptation of the digestive system to artificial diet, providing valuable insights for further research in the molecular domestic
    Pubmed: 37516099   DOI: 10.1016/j.cbd.2023.101112

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