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  • mProX™ Human SIK1 Stable Cell Line

    [CAT#: S01YF-1023-PY98]
    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-1222-KX487 Magic™ Human SIK(SNF1LK) in Vitro Assay Human Kinase Assay

    Product Information

    Target Family
    Kinases/Enzyme
    Target Protein Species
    Human
    Host Cell Type
    HEK293;CHO-K1;MHCC97H;SK-Hep1
    Target Classification
    Kinase Cell Lines
    Target Research Area
    Metabolic Research
    Related Diseases
    Developmental And Epileptic Encephalopathy 30; Early Myoclonic Encephalopathy
    Gene ID
    Human:150094
    UniProt ID
    Human:P57059

    Product Properties

    Biosafety Level
    Level 1
    Activity
    Yes
    Quantity
    10⁶ cells per vial
    Applications
    SIK1, or salt-inducible kinase 1, has been studied in various contexts and has shown potential applications in different fields. In the context of host-parasite interactions, SIK1 was found to be one of the differentially expressed genes in the spleen and liver of Eurasian perch infected with the pike tapeworm. The study suggests that SIK1 may play a role in the immune response of the host to the parasite. In the field of adipocyte biology, SIK1 was identified as one of the genes upregulated in subcutaneous white adipose tissue (scWAT) of patients with nonalcoholic fatty liver disease (NAFLD). Knockdown of SIK1 in adipocytes altered lipid metabolism and reduced lipid storage in hepatocytes in vitro. This suggests that SIK1 may be involved in the regulation of adipocyte function and could be a potential target for the treatment of NAFLD. In the field of neurobiology, knockdown of SIK3, a related kinase, in the CA1 region of the brain reduced seizure susceptibility in mice by inhibiting decreases in GABA(A)R α1 expression. This indicates that SIK3 may play a role in the development of epilepsy and could be a target for epilepsy treatment. In the field of cancer research, SIK1 was found to suppress colorectal cancer metastasis and chemoresistance via the TGF-β signaling pathway. The study suggests that SIK1 may be a potential therapeutic target for the treatment of colorectal cancer. Overall, SIK1 has shown diverse applications in different biological contexts, including host-parasite interactions, adipocyte biology, neurobiology, and cancer research.

    Protocols

    Please visit our protocols page.

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    FAQ

    chat Taylor Johnson (Verified Customer)

    How does SIK1 influence gastric cancer progression? Aug 21 2021

    chat Patrick Liam (Creative Biolabs Scientific Support)

    SIK1 acts as a tumor suppressor in gastric cancer by regulating δ-catenin protein stability and the miR-4449/SIK1 axis. Aug 21 2021

    chat Taylor Brown (Verified Customer)

    What is the role of SIK1 in osteosarcoma? Jan 29 2020

    chat Patrick Liam (Creative Biolabs Scientific Support)

    BMI1 promotes osteosarcoma cell proliferation and metastasis by inhibiting SIK1, making it a potential target for treatment. Jan 29 2020

    Published Data

    Fig.1 In vitro growth of HCC cell lines was significantly impeded by the robust inhibition exerted by SIK1.

    The lower panels display representative images of the entire plate, where the effects of SIK1 on the foci formation assay were assessed.

    Ref: Qu, Chao, et al. "Salt-inducible Kinase (SIK1) regulates HCC progression and WNT/β-catenin activation." Journal of hepatology 64.5 (2016): 1076-1089.

    Pubmed: 26778753

    DOI: 10.1016/j.jhep.2016.01.005

    Research Highlights

    Taube, Konrad. et al. "Subtle transcriptomic response of Eurasian perch ( Perca fluviatilis) associated with Triaenophorus nodulosus plerocercoid infection" International journal for parasitology. Parasites and wildlife, 2023.
    In order to better understand host-parasite interactions and their ecological and evolutionary implications, it is important to investigate the physiological effects of parasites and examine the genes involved in host responses to infections. However, this can be challenging due to the diverse nature and complex life cycles of many parasites. One way to address this issue is through the use of transcriptomics, which can provide qualitative and quantitative data on gene expression patterns in wild-caught specimens. In this study, the authors examined the physiological impact of the pike tapeworm (Triaenophorus nodulosus), a widely distributed parasite.
    Taube, Konrad. et al. "Subtle transcriptomic response of Eurasian perch ( Perca fluviatilis) associated with Triaenophorus nodulosus plerocercoid infection" International journal for parasitology. Parasites and wildlife, 2023.
    Pubmed: 37869060   DOI: 10.1016/j.ijppaw.2023.09.009

    Lopez-Yus, Marta. et al. "CRISPR/Cas9-mediated deletion of adipocyte genes associated with NAFLD alters adipocyte lipid handling and reduces steatosis in hepatocytes in vitro." American journal of physiology. Cell physiology, 2023.
    Obesity is a significant contributor to the development of nonalcoholic fatty liver disease (NAFLD). The primary lipid storage depot responsible for regulating lipid movement to other organs is the subcutaneous white adipose tissue (scWAT). Previous research has identified specific genes that are upregulated in the scWAT of individuals with NAFLD. These findings emphasize the crucial role of scWAT in the progression of NAFLD and highlight potential targets for therapeutic interventions.
    Lopez-Yus, Marta. et al. "CRISPR/Cas9-mediated deletion of adipocyte genes associated with NAFLD alters adipocyte lipid handling and reduces steatosis in hepatocytes in vitro." American journal of physiology. Cell physiology, 2023.
    Pubmed: 37721003   DOI: 10.1152/ajpcell.00291.2023

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