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  • mProX™ Human MARK2 Stable Cell Line

    [CAT#: S01YF-1123-KX300]
    Product Category:
    Membrane Protein Stable Cell Lines
    Subcategory:
    Kinase Cell Lines

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    Host Cell Type:
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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-KX1210 Magic™ Human MARK2 in Vitro Assay Human Kinase Assay

    Product Information

    Target Protein
    MARK2
    Target Family
    Kinases/Enzyme Drug Discovery Assays and Products
    Target Protein Species
    Human
    Host Cell Type
    U2-OS; CHO-K1; HEK293
    Target Classification
    Kinase Cell Lines
    Related Diseases
    Among its related pathways are Sertoli-Sertoli Cell Junction Dynamics and Complement cascade
    Gene ID
    UniProt ID

    Product Properties

    Biosafety Level
    Level 1
    Activity
    Yes
    Quantity
    10⁶ cells per vial
    Applications
    Kinase for serine/threonine proteins The MARK2 gene in humans codes for the enzyme MARK2. A small family of ser/thr protein kinases called EMK (ELKL Motif Kinase) is implicated in the regulation of cancer, microtubule stability, and cell polarity. Two isoforms of the human ser/thr protein kinase EMK1 have been encoded by a number of cDNA clones that have been identified. A 162-bp alternative exon that resulted in two forms-one with the exon and the other without-was what distinguished these isoforms. It was discovered that several chosen cell lines and tissue samples coexpressed both types. It has been demonstrated that a single mRNA that is widely expressed encodes the human EMK1. The customized MARK2 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 John

    I have been using the MARK2 KD cell line for my research, and it has consistently provided reliable results. Aug 10 2022

    chat Verified Customer

    chat Thomas

    The specificity and reproducibility of this MARK2 overexpression cell line are impressive. Apr 22 2020

    chat Verified Customer

    FAQ

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

    Published Data

    Fig.1 MARK2 regulates MT growth dynamics and orientation downstream of Rac1.

    Lysates from U2-OS cells transfected with non-targeting siRNA pool (lane 4), MARK2-shRNA (lane 2), control shRNA (lane 1), MARK2-shRNA (lane 2), and MARK2-shRNA and shRNA-resistant GFP-MARK2 (lane 3).

    Ref: Nishimura, Yukako, et al. "Automated screening of microtubule growth dynamics identifies MARK2 as a regulator of leading edge microtubules downstream of Rac1 in migrating cells." PloS one 7.7 (2012): e41413.

    Pubmed: 22848487

    DOI: 10.1371/journal.pone.0041413

    Research Highlights

    The information showed that MARK2/4 promotes metabolic reprogramming in NSCLC cells, which is how it causes cancer. As a result, MARK2/4 may be a viable target for lung cancer treatment.
    Natarajan, Sathan Raj, Lavanya Ponnusamy, and Ravi Manoharan. "MARK2/4 promotes Warburg effect and cell growth in non-small cell lung carcinoma through the AMPKα1/mTOR/HIF-1α signaling pathway." Biochimica et Biophysica Acta (BBA)-Molecular Cell Research 1869.7 (2022): 119242.
    Pubmed: 35192892   DOI: 10.1016/j.bbamcr.2022.119242

    In unperturbed mitosis and in response to antitubulin chemotherapy, MARK2 is phosphorylated by CDK1. MARK2 requires phosphorylation to control the course of mitosis and the cytotoxicity of paclitaxel in PDAC cells.
    Zeng, Yongji, et al. "MARK2 regulates chemotherapeutic responses through class IIa HDAC-YAP axis in pancreatic cancer." Oncogene 41.31 (2022): 3859-3875.
    Pubmed: 35780183   DOI: 10.1038/s41388-022-02399-3

    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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