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  • mProX™ Human RPS6KA2 Stable Cell Line

    [CAT#: S01YF-1023-PY93]
    Product Category:
    Membrane Protein Stable Cell Lines
    Subcategory:
    Kinase 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-1222-KX482 Magic™ Human RSK3(RPS6KA2) in Vitro Assay Human Kinase Assay

    Product Information

    Target Family
    Kinases/Enzyme
    Target Protein Species
    Human
    Host Cell Type
    HEK293;CHO-K1;SK-OV-3;OVCAR-3
    Target Classification
    Kinase Cell Lines
    Target Research Area
    Pain and Addiction Research
    Related Diseases
    Coffin-Lowry Syndrome
    Gene ID
    Human:6196
    UniProt ID
    Human:Q15349

    Product Properties

    Biosafety Level
    Level 1
    Activity
    Yes
    Quantity
    10⁶ cells per vial
    Applications
    RPS6KA2, also known as ribosomal protein S6 kinase A2, has been studied in various contexts. In ovarian cancer, RPS6KA2 is involved in cuproptosis, a form of programmed cell death, and its related long non-coding RNAs (lncRNAs) have been characterized. These lncRNAs have been used to define molecular subtypes of ovarian cancer and establish a prognostic signature that can predict survival time, immune characteristics, and response to therapy. In Crohn's disease, RPS6KA2 is associated with DNA methylation alterations that may predict disease recurrence following intestinal resection. In knee osteoarthritis, RPS6KA2 enhances the chondrogenic differentiation of induced mesenchymal stem cells (iMSCs), leading to articular cartilage regeneration. In Yorkshire pigs, RPS6KA2 is one of the candidate genes identified in a genome-wide association study on reproductive traits. Finally, in food allergy, epigenome-wide association studies have found DNA methylome variations in RPS6KA2 and other genes associated with immune responses and regulatory T cell function. These findings provide insights into the role of RPS6KA2 in different diseases and highlight its potential as a therapeutic target or biomarker.

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    FAQ

    chat Casey Miller (Verified Customer)

    What is the role of RPS6KA2 in osteosarcoma? Aug 04 2023

    chat Patrick Liam (Creative Biolabs Scientific Support)

    Downregulation of RPS6KA2 is associated with the inhibition of osteosarcoma proliferation, suggesting its potential as a therapeutic target. Aug 04 2023

    chat Jordan Brown (Verified Customer)

    How does RPS6KA2 affect ovarian cancer? Jan 09 2022

    chat Patrick Liam (Creative Biolabs Scientific Support)

    Low expression of RPS6KA2, mediated by specific ncRNAs, can influence the proliferation of ovarian cancer cells via the p38/MAPK signaling pathway. Jan 09 2022

    Published Data

    Fig.1 The proliferation of ovarian cancer cells was inhibited by RPS6KA2.

    In the investigation of the inhibitory effects of RPS6KA2 on ovarian cancer cell proliferation, a CCK-8 assay was carried out. It was observed that in comparison to the control cells, a reduction in cell viability of ovarian cancer cells was induced by the OE group of OVCAR3 cells. Conversely, the proliferation of ovarian cancer cells was promoted when SKOV3 cells were transfected with RPS6KA2 shRNA.

    Ref: Fu, Zhiqin, et al. "ncRNAs mediated RPS6KA2 inhibits ovarian cancer proliferation via p38/MAPK signaling pathway." Frontiers in Oncology 13 (2023): 1028301.

    Pubmed: 36741009

    DOI: 10.3389/fonc.2023.1028301

    Research Highlights

    Li, Nan. et al. "Molecular Characterization of Cuproptosis-related lncRNAs: Defining Molecular Subtypes and a Prognostic Signature of Ovarian Cancer." Biological trace element research, 2023.
    A recently discovered form of programmed cell death known as Cuproptosis has been found to be altered in women with ovarian cancer. In order to further understand the effects of Cuproptosis on ovarian cancer, researchers conducted a study using data from various databases and analyzed the expression of specific genes and long non-coding RNAs (lncRNAs). Through their analysis, the researchers were able to identify four molecular subtypes of ovarian cancer based on Cuproptosis-related lncRNAs, which differed in survival time, immune characteristics, and somatic mutation. Furthermore, a prognostic signature consisting of 10 lncRNAs was established and found to be significantly correlated with prognosis, immune microenvironment, and response to certain treatments. Additional experiments on different ovarian cancer cell lines also supported the potential role of these lncRNAs in tumor growth and response to treatment. This study sheds light on the heterogeneity of ovarian cancer and offers new insights on its prognosis and immune microenvironment, with potential clinical benefits for patients.
    Li, Nan. et al. "Molecular Characterization of Cuproptosis-related lncRNAs: Defining Molecular Subtypes and a Prognostic Signature of Ovarian Cancer." Biological trace element research, 2023.
    Pubmed: 37528285   DOI: 10.1007/s12011-023-03780-3

    T Ventham, Nicholas. et al. "Genome-Wide Methylation Profiling in 229 Patients With Crohn's Disease Requiring Intestinal Resection: Epigenetic Analysis of the Trial of Prevention of Post-operative Crohn's Disease (TOPPIC)." Cellular and molecular gastroenterology and hepatology, 2023.
    The study focuses on the potential role of DNA methylation alterations in gene-environment interaction in diverse health conditions, including cancer, aging, and inflammatory bowel disease (IBD). The researchers aim to investigate whether changes in the DNA methylome of patients undergoing surgery can predict the recurrence of Crohn's disease (CD) after intestinal resection. Additionally, they plan to compare the circulating methylome of patients with established CD with that reported in previous studies involving inception cohorts.
    T Ventham, Nicholas. et al. "Genome-Wide Methylation Profiling in 229 Patients With Crohn's Disease Requiring Intestinal Resection: Epigenetic Analysis of the Trial of Prevention of Post-operative Crohn's Disease (TOPPIC)." Cellular and molecular gastroenterology and hepatology, 2023.
    Pubmed: 37331566   DOI: 10.1016/j.jcmgh.2023.06.001

    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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