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  • mProX™ Human CDK6 Stable Cell Line

    [CAT#: S01YF-1123-KX188]
    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-KX1073 Magic™ Human CDK6/CycD1 in Vitro Assay Human Kinase Assay
    S01YF-1122-KX1074 Magic™ Human CDK6/CycD3 in Vitro Assay Human Kinase Assay

    Product Information

    Target Protein
    CDK6
    Target Family
    Kinases/Enzyme Drug Discovery Assays and Products
    Target Protein Species
    Human
    Host Cell Type
    COLO320; CHO-K1; HEK293
    Target Classification
    Kinase Cell Lines
    Target Research Area
    Reproductive Research
    Related Diseases
    Microcephaly 12, Primary, Autosomal Recessive and Primary Autosomal Recessive Microcephaly. Among its related pathways are Aberrant regulation of mitotic G1/S transition in cancer due to RB1 defects and Evasion of Oxidative Stress Induced Senescence Due to Defective p16INK4A binding to CDK4 and CDK6
    Gene ID
    UniProt ID

    Product Properties

    Biosafety Level
    Level 1
    Activity
    Yes
    Quantity
    10⁶ cells per vial
    Applications
    The enzyme known as cell division protein kinase 6 (CDK6) is produced by the CDK6 gene. This gene codes for a protein that is a part of the CDK (cyclin-dependent kinase) family, which also contains CDK4. This kinase is a catalytic subunit of the protein kinase complex, which is also made up of the activating subunit cyclin D. The complex is crucial for the G1 phase advancement and G1/S transition of the cell cycle. Mid-G1 phase, when this kinase's activity initially manifests, is regulated by components such as D-type cyclins and CDK inhibitors belonging to the INK4 family. CDK6 is a crucial protein in cancer since it has been demonstrated that this kinase and CDK4 phosphorylate the tumor suppressor Retinoblastoma protein, hence controlling its activity. The customized CDK6 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 Elizabeth

    This human CDK6 cell line is highly selective. Its performance has been outstanding, demonstrating reliable and consistent binding. Mar 10 2022

    chat Verified Customer

    chat Linda

    This CDK6 cell line can be applied well according to experimental needs. Dec 02 2022

    chat Verified Customer

    FAQ

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

    Published Data

    Fig.1 CDK6 phosphorylates RB for cancer cell growth.

    Lentivral vectors expressing CDK4 shRNA sequences (CDK4-20, CDK4-64) and CDK6 shRNA sequences (CDK6-893, CDK6-747) were used to transduce COLO320 cells. The cells were then subjected to western blotting with the antibodies as stated (left of panel).

    Ref: Li, Chunsheng, et al. "PD‑0332991 induces G1 arrest of colorectal carcinoma cells through inhibition of the cyclin‑dependent kinase‑6 and retinoblastoma protein axis." Oncology letters 7.5 (2014): 1673-1678.

    Pubmed: 24765199

    DOI: 10.3892/ol.2014.1957

    Research Highlights

    Cyclin-dependent kinase 6 (CDK6) is essential for controlling how the cell cycle develops. It has also been demonstrated more recently that CDK6 plays a transcriptional role in tumor angiogenesis.
    Tadesse, Solomon, et al. "Targeting CDK6 in cancer: State of the art and new insights." Cell Cycle 14.20 (2015): 3220-3230.
    Pubmed: 26315616   DOI: 10.1080/15384101.2015.1084445

    Both hematopoietic stem cells and tumor cells use CDK6 directly for transcription. These activities suggest that CDK6 has a role in tissue homeostasis and differentiation that is distinct from CDK4 and partially independent of CDK6 kinase activity.
    Tigan, A. S., et al. "CDK6-a review of the past and a glimpse into the future: from cell-cycle control to transcriptional regulation." Oncogene 35.24 (2016): 3083-3091.
    Pubmed: 26500059   DOI: 10.1038/onc.2015.407

    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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