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  • mProX™ Human PROKR1 Stable Cell Line

    [CAT#: S01YF-0923-KX1]
    Product Category:
    Membrane Protein Stable Cell Lines
    Subcategory:
    GPCR Cell Lines

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    Product Information

    Target Protein
    PROKR1
    Target Family
    Prokineticin Family
    Target Protein Species
    Human
    Host Cell Type
    CHO-K1; HEK293T
    Target Classification
    GPCR Cell Lines
    Target Research Area
    Cardiovascular Research; Inflammation Research
    Related Diseases
    Hirschsprung Disease; Kallmann Syndrome
    Gene ID
    UniProt ID

    Product Properties

    Biosafety Level
    Level 1
    Activity
    Yes
    Quantity
    10⁶ cells per vial
    Applications
    Adipose tissue and the cardiovascular system both benefit from prokineticin receptor 1 (Prokr1)'s improved metabolic profile; however, its effects on skeletal muscle have not been studied. We looked at the metabolic role of Prokr1 in the murine myoblast, satellite cells, and their developed myotubes. We examined the Prokr1 expression levels in both human skeletal muscle cell-derived myotubes and mouse skeletal muscle. In HEK293T cells that had PROKR1 overexpressed, prokineticin 2 (PROK2), a ligand of PROKR1, changed the mRNA levels of 578 genes and dose-dependently increased calcium mobilization. In skeletal muscle cells, PROKR1 stimulated Gq-mediated PI3K/AKT and MAPK/ERK signaling pathways, according to functional enrichment analysis of differentially expressed genes. In myotubes generated from C2C12 and satellite cells, Prokr1 dramatically stimulated the PI3K/AKT signaling pathway, regardless of the presence or absence of insulin. Glucose transporter 4 (GLUT4) was also helped enter the plasma membrane by Prokr1. Prokr1 improved insulin-stimulated AKT phosphorylation, GLUT4 translocation, and glucose uptake in myotubes that had developed insulin resistance due to palmitate. The customized PROKR1 stable cell line can be used in antibody discovery and development, potential drug candidate screening and signaling pathway researches.

    Protocols

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    FAQ

    chat Jacqueline (Verified Customer)

    Is the receptor in my product full length? Feb 03 2023

    chat Sherry Smith (Creative Biolabs Scientific Support)

    The amino acids that were included are indicated if an amino acid range is given. If there is no listed range of amino acids, the receptor's entire length was used. Feb 03 2023

    chat Jean (Verified Customer)

    Is transgene expression measured by flow cytometry? Aug 30 2023

    chat Sherry Smith (Creative Biolabs Scientific Support)

    Our cell lines from which expression data was generated via flow cytometry analysis. Aug 30 2023

    Published Data

    Fig.1 Signaling pathways of PROKR1.

    Expression analysis of PROKR1 overexpression in HEK293T cells, PROKR1 mRNA and protein in HEK293T cells, mock control with an empty vector, and blank control.

    Ref: Mok, Jongsoo, et al. "Prokineticin receptor 1 ameliorates insulin resistance in skeletal muscle." The FASEB Journal 35.2 (2021): e21179.

    Pubmed: 33184929

    DOI: 10.1096/fj.202001641R

    Research Highlights

    The distribution of PROKR1 protein by CDVs made from genetically modified cells seems to be a successful procedure, and they show promise as an alternative treatment for muscular dystrophy.
    Zhang, Chunjuan, et al. "PROKR1 delivery by cell-derived vesicles restores the myogenic potential of Prokr1-deficient C2C12 myoblasts." Nanomedicine: Nanotechnology, Biology and Medicine 37 (2021): 102448.
    Pubmed: 34314870   DOI: 10.1016/j.nano.2021.102448

    In order to identify the expression of PROK 1 and PROKR 1 in endometriosis-related eutopic and ectopic endometrium as well as normal control endometrium, quantitative real-time PCR (qPCR) and Western blotting were used. The development of endometriosis and its pathophysiology are influenced by PROK-1 and its receptors. TNF-α can stimulate angiogenesis by increasing PROK 1 expression.
    Wu, Yahong, and Xianqing Wu. "Expression of PROK 1 and its receptor PROKR 1 in endometriosis and its clinical significance." Journal of Central South University. Medical Sciences 44.6 (2019): 621-627.
    Pubmed: 31304922   DOI: 10.11817/j.issn.1672-7347.2019.06.003

    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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