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  • mProX™ Human DYRK1A Stable Cell Line

    [CAT#: S01YF-1123-KX217]
    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-KX1104 Magic™ Human DYRK1A in Vitro Assay Human Kinase Assay

    Product Information

    Target Protein
    DYRK1A
    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
    Reproductive Research
    Related Diseases
    Intellectual Developmental Disorder, Autosomal Dominant 7 and Dyrk1a-Related Intellectual Disability Syndrome. Among its related pathways are "Cell Cycle, Mitotic" and Mitotic G1 phase and G1/S transition
    Gene ID
    UniProt ID

    Product Properties

    Biosafety Level
    Level 1
    Activity
    Yes
    Quantity
    10⁶ cells per vial
    Applications
    Instructions for producing an enzyme crucial to the nervous system's development are provided by the DYRK1A gene. The DYRK1A enzyme is a kinase, which means that it phosphorylates other proteins by adding a cluster of atoms containing phosphorus and oxygen. The proteins that the DYRK1A enzyme aids in regulating are involved in a number of cellular activities. The DYRK1A enzyme is involved in the development of dendritic spines from dendrites in nerve cells. The transmission of nerve impulses depends on dendrites, which are specialized extensions from neurons. Small projections from dendrites called dendritic spines aid in nerve impulse transmission and improve neuronal communication. The customized DYRK1A 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 Karen

    I am truly impressed with the performance of this DYRK1A cell line and the professionalism of Creative Biolabs. I highly recommend it to anyone. Mar 15 2022

    chat Verified Customer

    chat Christopher

    I purchased the DYRK1A cell line from Creative Biolabs. The provided documentation was comprehensive and helped me optimize my assay conditions. Jan 03 2020

    chat Verified Customer

    FAQ

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

    Published Data

    Fig.1 DYRK1A co-purifies with p300 and CBP.

    After creating a clonal HEK293 cell line that inducibly expressed Flag-DYRK1A, nuclear extracts were produced and then affinity purified. Mass spectrometry and SDS-PAGE were used to analyze the luates. The position of DYRK1A in the silver-stained gel is shown by an arrow.

    Ref: Li, Shanshan, et al. "DYRK1A interacts with histone acetyl transferase p300 and CBP and localizes to enhancers." Nucleic acids research 46.21 (2018): 11202-11213.

    Pubmed: 30137413

    DOI: 10.1093/nar/gky754

    Research Highlights

    They concentrate on DYRK1A's properties, regulation, and functional relevance in various human disorders, which brings us to a summary of upcoming studies on this protein with exciting therapeutic potential.
    Deboever, Estelle, et al. "The omnipresence of DYRK1A in human diseases." International journal of molecular sciences 23.16 (2022): 9355.
    Pubmed: 36012629   DOI: 10.3390/ijms23169355

    The importance of DYRK1A in a variety of illnesses is further supported by the significant efforts being made in drug development to create strong and specific DYRK1A inhibitors. Recently, a number of classes of DYRK1A inhibitors have been identified, and some of these compounds show promise for the development of DYRK1A inhibitors as medications for DYRK1A-dependent illnesses.
    Abbassi, Ramzi, et al. "DYRK1A in neurodegeneration and cancer: Molecular basis and clinical implications." Pharmacology & therapeutics 151 (2015): 87-98.
    Pubmed: 25795597   DOI: 10.1016/j.pharmthera.2015.03.004

    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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