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  • mProX™ Human CHUK Stable Cell Line

    [CAT#: S01YF-1123-KX263]
    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-KX1168 Magic™ Human IKK-alpha in Vitro Assay Human Kinase Assay

    Product Information

    Target Protein
    CHUK
    Target Family
    Kinases/Enzyme Drug Discovery Assays and Products
    Target Protein Species
    Human
    Host Cell Type
    H1437; CHO-K1; HEK293
    Target Classification
    Kinase Cell Lines
    Target Research Area
    Reproductive Research
    Related Diseases
    Fetal Encasement Syndrome and Bartsocas-Papas Syndrome 2. Among its related pathways are MyD88 dependent cascade initiated on endosome and TNFR1 Pathway
    Gene ID
    UniProt ID

    Product Properties

    Biosafety Level
    Level 1
    Activity
    Yes
    Quantity
    10⁶ cells per vial
    Applications
    Nuclear factor inhibitor The CHUK gene in humans encodes kappa-B kinase subunit alpha (IKK-α), which is sometimes referred to as IKK1 or conserved helix-loop-helix ubiquitous kinase (CHUK). The IκB kinase complex, which includes IKK-α, is crucial for controlling the NF-κB transcription factor. Nevertheless, IKK-α is believed to regulate epidermal differentiation independently of the NF-κB pathway and has numerous other cellular targets. The potential therapeutic benefit of inhibiting IκB kinase (IKK) and IKK-related kinases, such as IKBKE (IKKε) and TANK-binding kinase 1 (TBK1), has been explored for the management of cancer and inflammatory disorders. The customized CHUK 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 James

    I've been using the mouse CHUK overexpression cell line for my studies. May 19 2021

    chat Verified Customer

    chat Anthony

    The CHUK overexpression cell line showed good performance in our hands. Feb 20 2020

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    FAQ

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

    Published Data

    Fig.1 Generation of IKKα knockdown human NSCLC cell lines.

    In each of the human NSCLC lines stably transduced with the Dox-inducible IKKα shRNA lentiviral vector, Western blots demonstrate the loss of IKKα protein expression in response to Dox treatment. In contrast, IKKα protein levels remain wild type (WT) in the same NSCLC lines stably transduced with an empty lentiviral vector control lacking the IKKα shRNA insert (IKKαWT-lentiviral vector controls).

    Ref: Chavdoula, Evangelia, et al. "CHUK/IKK-α loss in lung epithelial cells enhances NSCLC growth associated with HIF up-regulation." Life science alliance 2.6 (2019).

    Pubmed: 31792060

    DOI: 10.26508/lsa.201900460

    Research Highlights

    The phrase CHUK plays a role in the evolution of IS. Patients with IS may have changes in blood pressure and cholesterol levels due to CHUK mutations rs2230804 and rs3808917. The polymorphisms for CHUK rs3808916, rs2230804, and rs3808917, however, are not linked to an increased risk of IS.
    Huang, Jingyan, et al. "Association of CHUK gene polymorphism and ischemic stroke in the Han Chinese population." Journal of Clinical Neuroscience 88 (2021): 271-276.
    Pubmed: 33992196   DOI: 10.1016/j.jocn.2021.04.009

    The aim of the study was to examine the potential anti-cancer effects and underlying molecular mechanisms of cytostasis induced by the anti-microtubule medication ABT-751 in two genetically divergent urinary bladder urothelial carcinoma (UBUC)-derived cell lines, BFTC905 and J82.
    Dehghanian, Seyedeh Zahra, et al. "ABT-751 induces multiple anticancer effects in urinary bladder urothelial carcinoma-derived cells: Highlighting the induction of cytostasis through the inhibition of SKP2 at both transcriptional and post-translational levels." International journal of molecular sciences 22.2 (2021): 945.
    Pubmed: 33478005   DOI: 10.3390/ijms22020945

    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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