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  • mProX™ Human CDK19 Stable Cell Line

    [CAT#: S01YF-1123-KX183]
    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-1122-KX1065 Magic™ Human CDK19/CycC in Vitro Assay Human Kinase Assay

    Product Information

    Target Protein
    CDK19
    Target Family
    Kinases/Enzyme Drug Discovery Assays and Products
    Target Protein Species
    Human
    Host Cell Type
    CHO-K1; HEK293
    Target Classification
    Kinase Cell Lines
    Target Research Area
    CNS Research; Inflammation Research
    Related Diseases
    Developmental And Epileptic Encephalopathy 87 and Non-Specific Early-Onset Epileptic Encephalopathy. Among its related pathways are PPARA activates gene expression and Metabolism
    Gene ID
    UniProt ID

    Product Properties

    Biosafety Level
    Level 1
    Activity
    Yes
    Quantity
    10⁶ cells per vial
    Applications
    Although CDK19 is conserved in model organisms that are both vertebrate and invertebrate, defects in CDK19 are not currently linked to any disorders in humans. Larval lethality is caused by loss of Cdk8, the fly homolog of CDK19, and is prevented by expression of the human CDK19 reference cDNA. Conversely, the CDK19 p.Tyr32His and p.Thr196Ala variations found in the afflicted people act as null alleles and are unable to compensate for the loss of Cdk8. Furthermore, semi-lethality is the outcome of Cdk8 knockdown in flies using neuronal RNAi. The few flies that eclose show signs of severe seizures and a shorter life span. Moderate expression of the CDK19 standard cDNA completely suppresses both symptoms, whereas expression of the two variations does not. The customized CDK19 stable cell line can be used in antibody discovery and development, potential drug candidate screening and signaling pathway researches.

    Protocols

    Please visit our protocols page.

    Customer Reviews

    chat Jennifer

    We obtained good data in downstream analysis using this CDK19 cell line. May 07 2023

    chat Verified Customer

    chat Brian

    A good CDK19 cell line. The company obtains a wide range of membrane protein products which are very reliable. Aug 18 2022

    chat Verified Customer

    FAQ

    Any questions about our products? Please visit our frequently asked questions page.

    Published Data

    Fig.1 CDK8/19 kinase activity is necessary for intestinal epithelial cell intrinsic growth and differentiation.

    Small intestine organoids from mice treated with 4-OHT for 24 hours, one week later, were immunoblotted from VillinCreER T2, VillinCreER T2 /Cdk8 fl/fl, and VillinCreER T2 /Cdk8 fl/fl /Cdk19 -/-mice.

    Ref: Dannappel, Marius V., et al. "CDK8 and CDK19 regulate intestinal differentiation and homeostasis via the chromatin remodeling complex SWI/SNF." The Journal of clinical investigation 132.20 (2022).

    Pubmed: 36006697

    DOI: 10.1172/JCI158593

    Research Highlights

    Known together as "Mediator Kinases," CDK8 and its paralog, CDK19, are cyclin-dependent kinases that have been identified as important regulators of cellular homeostasis and developmental programming.
    Dannappel, Marius Volker, et al. "Molecular and in vivo functions of the CDK8 and CDK19 kinase modules." Frontiers in cell and developmental biology 6 (2019): 171.
    Pubmed: 30693281   DOI: 10.3389/fcell.2018.00171

    While CDK8 and CDK19 have similar qualitative effects on gene expression at the RNA and protein levels and on protein phosphorylation, analysis of isogenic cell populations expressing CDK8, CDK19, or their kinase-inactive mutants showed that the differences in the effects of CDK8 versus CDK19 knockouts were due to quantitative variations in their expression and activity rather than distinct functions.
    Chen, Mengqian, et al. "CDK8 and CDK19: positive regulators of signal-induced transcription and negative regulators of Mediator complex proteins." Nucleic Acids Research 51.14 (2023): 7288-7313.
    Pubmed: 37378433   DOI: 10.1093/nar/gkad538

    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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