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  • mProX™ Human ALK Stable Cell Line

    [CAT#: S01YF-1123-KX148]
    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-KX1026 Magic™ Human ALK in Vitro Assay Human Kinase Assay
    S01YF-1122-KX1027 Magic™ Human ALK[G1202R] in Vitro Assay Human Kinase Assay

    Product Information

    Target Protein
    ALK
    Target Family
    Kinases/Enzyme Drug Discovery Assays and Products
    Target Protein Species
    Human
    Host Cell Type
    SH-SY5Y; CHO-K1; HEK293
    Target Classification
    Kinase Cell Lines
    Target Research Area
    Cancer Research
    Related Diseases
    Neuroblastoma 3 and Neuroblastoma. Among its related pathways are Pluripotent stem cell differentiation pathway and Signaling by ALK in cancer
    Gene ID
    UniProt ID

    Product Properties

    Biosafety Level
    Level 1
    Activity
    Yes
    Quantity
    10⁶ cells per vial
    Applications
    ALK receptor tyrosine kinase, a member of the receptor tyrosine kinase (RTK) family of proteins, is made using instructions derived from the ALK gene. The kinase binds to a comparable kinase after being activated at the cell surface to initiate the process. Phosphorylation is the process by which the kinase is marked with a phosphate group following dimerization. The kinase is activated by phosphorylation. Another protein in the cell can get a phosphate group from the activated kinase, activating it in the process. A signaling pathway's sequence of proteins carry on the activation. Numerous biological activities, including cell growth, division, and maturation, depend on these signaling pathways. The customized ALK 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 Jacqueline

    I highly recommend the ALK cell line for anyone working on membrane protein research. Feb 03 2023

    chat Verified Customer

    chat Jean

    The ALK cell line proved to be an invaluable tool in my experiments. Its excellent performance and reproducibility greatly contributed to the success of my research project. Aug 30 2023

    chat Verified Customer

    FAQ

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

    Published Data

    Fig.1 ALK inhibitors inhibit or partially inhibit the proliferation of neuroblastoma cell lines harboring ALK aberrations.

    Dose response curves of neuroblastoma cell lines with ALK mutations or increased expression subjected to ceritinib, crizotinib, alectinib, and PF06463922, four ALK inhibitors.

    Ref: Wang, Hui Qin, et al. "Combined ALK and MDM2 inhibition increases antitumor activity and overcomes resistance in human ALK mutant neuroblastoma cell lines and xenograft models." Elife 6 (2017): e17137.

    Pubmed: 28425916

    DOI: 10.7554/eLife.17137

    Research Highlights

    When treating ALK-positive non-small-cell lung cancer (NSCLC), alexib, a highly selective inhibitor of anaplastic lymphoma kinase (ALK), has demonstrated systemic and central nervous system (CNS) efficacy.
    Peters, Solange, et al. "Alectinib versus crizotinib in untreated ALK-positive non-small-cell lung cancer." New England Journal of Medicine 377.9 (2017): 829-838.
    Pubmed: 28586279   DOI: 10.1056/NEJMoa1704795

    When crizotinib was no longer effective for treating patients with ALK-positive NSCLC, alexitab demonstrated clinical activity and was well tolerated. Therefore, individuals with ALK-positive illness who have not responded well to crizotinib may benefit from alectinib therapy.
    Shaw, Alice T., et al. "Alectinib in ALK-positive, crizotinib-resistant, non-small-cell lung cancer: a single-group, multicentre, phase 2 trial." The lancet oncology 17.2 (2016): 234-242.
    Pubmed: 26708155   DOI: 10.1016/S1470-2045(15)00488-X

    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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