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  • mProX™ Human DMPK Stable Cell Line

    [CAT#: S01YF-1123-KX215]
    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-KX1102 Magic™ Human DMPK1(DMPK) in Vitro Assay Human Kinase Assay

    Product Information

    Target Protein
    DMPK
    Target Family
    Kinases/Enzyme Drug Discovery Assays and Products
    Target Protein Species
    Human
    Host Cell Type
    SAOS-2; CHO-K1; HEK293
    Target Classification
    Kinase Cell Lines
    Target Research Area
    CNS Research; Reproductive Research
    Related Diseases
    Myotonic Dystrophy 1 and Congenital-Onset Steinert Myotonic Dystrophy. Among its related pathways are Cardiac conduction and G-protein signaling RAC1 in cellular process
    Gene ID
    UniProt ID

    Product Properties

    Biosafety Level
    Level 1
    Activity
    Yes
    Quantity
    10⁶ cells per vial
    Applications
    Instructions for producing a protein known as myotonic dystrophy protein kinase are found in the DMPK gene. It seems that this protein is crucial for heart, brain, and muscle cells. The protein might have a role in cell-to-cell communication. Via interactions with other proteins, it also seems to control the synthesis and operation of key structures within muscle cells. A set of three repeating DNA building blocks can be found in one area of the DMPK gene. This sequence is referred to as a triplet or trinucleotide repeat and is written as CTG. The majority of persons have between five and thirty-four CTG repeats in this gene. The customized DMPK 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 Amy

    The DMPK cell line was easy to use, and the customer service team was responsive and helpful. Highly recommended! Jun 05 2022

    chat Verified Customer

    chat Robert

    The technical support team was knowledgeable and provided prompt assistance whenever we had questions. I am extremely satisfied with this DMPK cell line and the overall experience. Feb 27 2022

    chat Verified Customer

    FAQ

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

    Published Data

    Fig.1 Human DMPK-A associates with the mitochondria and its kinase activity prevents ROS-induced cell death.

    Expression of hDMPK-A in human osteosarcoma SAOS-2 cells that have been transfected stably with plasmids either a wild-type or a fake construct The KD or hDMPK-A hDMPK-A variation. The western immunoblot's loading control was GAPDH.

    Ref: Pantic, B., et al. "Myotonic dystrophy protein kinase (DMPK) prevents ROS-induced cell death by assembling a hexokinase II-Src complex on the mitochondrial surface." Cell death & disease 4.10 (2013): e858-e858.

    Pubmed: 24136222

    DOI: 10.1038/cddis.2013.385

    Research Highlights

    A newer technique is targeted protein degraders. Their properties are in the 'beyond rule of 5' space, which is distinct from the standard small-molecule property space. As a result, in contrast to conventional small molecules, drug development initiatives aimed at creating orally accessible degraders are anticipated to encounter challenging drug metabolism and pharmacokinetics (DMPK) issues.
    Cantrill, Carina, et al. "Fundamental aspects of DMPK optimization of targeted protein degraders." Drug Discovery Today 25.6 (2020): 969-982.
    Pubmed: 32298797   DOI: 10.1016/j.drudis.2020.03.012

    A clear workflow for DMPK tasks was created, starting with early lead discovery and ending with the choice of a potential medication. This led to a chemical series optimization that was both economical and successful, and it made it easier to make wise decisions as the project moved forward.
    Sohlenius-Sternbeck, Anna-Karin, et al. "Optimizing DMPK properties: experiences from a Big Pharma DMPK department." Current Drug Metabolism 17.3 (2016): 253-270.
    Pubmed: 26651977   DOI: 10.2174/1389200217666151210125637

    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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