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  • mProX™ Human CSK Stable Cell Line

    [CAT#: S01YF-1123-KX209]
    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-KX1096 Magic™ Human CSK in Vitro Assay Human Kinase Assay

    Product Information

    Target Protein
    CSK
    Target Family
    Kinases/Enzyme Drug Discovery Assays and Products
    Target Protein Species
    Human
    Host Cell Type
    CHO-K1; HEK293
    Target Classification
    Kinase Cell Lines
    Target Research Area
    Autoimmune Research
    Related Diseases
    Osteopetrosis and Lupus Erythematosus. Among its related pathways are Signaling downstream of RAS mutants and RAF/MAP kinase cascade.
    Gene ID
    UniProt ID

    Product Properties

    Biosafety Level
    Level 1
    Activity
    Yes
    Quantity
    10⁶ cells per vial
    Applications
    Kinase tyrosine-protein C-terminal is another name for CSK. The CSK gene in humans codes for the enzyme src kinase. Tyrosine residues in the C-terminal end of Src-family kinases (SFKs) are phosphorylated by this enzyme. The control of cell proliferation, differentiation, migration, and immunological response is significantly influenced by this non-receptor tyrosine-protein kinase. By phosphorylating members of the Src family of protein kinases at a conserved C-terminal tail location in Src, CSK inhibits the activity of the Src family of protein kinases. In order to block SFKs, CSK is first drawn to the plasma membrane by attaching itself to transmembrane proteins or adaptor proteins that are in close proximity to the membrane. By phosphorylating and keeping inactive a number of effector molecules, CSK then suppresses signaling through a variety of surface receptors. The customized CSK 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 Donna

    The CSK cell line has not disappointed. It consistently delivers accurate results, making my work much more impactful. May 08 2023

    chat Verified Customer

    chat Christopher

    The protocol of CSK cell line was straightforward, and the results were consistent. Apr 21 2020

    chat Verified Customer

    FAQ

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

    Published Data

    Fig.1 Comparison of the expression levels of CHK versus Csk in human neuroblastoma cell lines.

    Comparative analysis using Western blotting of CHK and Csk expression levels in human neuroblastoma cell lines. Be(2)c cells and newly generated neuroblastoma cell lines, designated as 5425, 4030.2, 4181, and 9080.

    Ref: Zagozdzon, Radoslaw, Yigong Fu, and Hava Karsenty Avraham. "Csk homologous kinase inhibits CXCL12-CXCR4 signaling in neuroblastoma." International journal of oncology 32.3 (2008): 619-623.

    Pubmed: 18292939

    Research Highlights

    The Src-family protein tyrosine kinases (SFKs) are naturally inhibited by C-terminal Src kinase (CSK) and CSK-homologous kinase (CHK). Because constitutive activation of SFKs is linked to the development and spread of cancer, CSK and CHK regulate SFK activity in normal cells to keep it at a basal level.
    Chong, Yuh-Ping, Terrence D. Mulhern, and Heung-Chin Cheng. "C-terminal Src kinase (CSK) and CSK-homologous kinase (CHK)-endogenous negative regulators of Src-family protein kinases: Mini Review." Growth factors 23.3 (2005): 233-244.
    Pubmed: 16243715   DOI: 10.1080/08977190500178877

    The essential enzymes for mammalian signal transduction are protein tyrosine kinases (PTK). Each PTK phosphorylates a single or small number of proteins on particular Tyr residues in order to maintain the integrity of signal transduction.
    Lee, Sungsoo, et al. "Determination of the substrate-docking site of protein tyrosine kinase C-terminal Src kinase." Proceedings of the National Academy of Sciences 100.25 (2003): 14707-14712.
    Pubmed: 14657361   DOI: 10.1073/pnas.2534493100

    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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