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p p70 s6 kinase  (Cell Signaling Technology Inc)


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    Structured Review

    Cell Signaling Technology Inc p p70 s6 kinase
    P P70 S6 Kinase, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 97/100, based on 4218 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/p+s6+antibody/p70+S6+Kinase+Antibody/pm41904172-63-14-28
    Average 97 stars, based on 4218 article reviews
    p p70 s6 kinase - by Bioz Stars, 2026-09
    97/100 stars

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    Related Articles

    Staining:

    Article Title: IL-37d suppresses Rheb-mTORC1 axis independently of TCS2 to alleviate alcoholic liver disease.
    Article Snippet: .. For intracellular cytokine staining, cells were incubated in 100 μl p-S6K or p-S6 antibody (clone #4851, Cell Signaling Technology, Danvers, USA) diluent for 1 h. The dilution concentration of the antibody is 1:50. ..

    Article Title: IL-37d suppresses Rheb-mTORC1 axis independently of TCS2 to alleviate alcoholic liver disease
    Article Snippet: .. For intracellular cytokine staining, cells were incubated in 100 μl p-S6K or p-S6 antibody (clone #4851, Cell Signaling Technology, Danvers, USA) diluent for 1 h. The dilution concentration of the antibody is 1:50. ..

    Incubation:

    Article Title: IL-37d suppresses Rheb-mTORC1 axis independently of TCS2 to alleviate alcoholic liver disease.
    Article Snippet: .. For intracellular cytokine staining, cells were incubated in 100 μl p-S6K or p-S6 antibody (clone #4851, Cell Signaling Technology, Danvers, USA) diluent for 1 h. The dilution concentration of the antibody is 1:50. ..

    Article Title: IL-37d suppresses Rheb-mTORC1 axis independently of TCS2 to alleviate alcoholic liver disease
    Article Snippet: .. For intracellular cytokine staining, cells were incubated in 100 μl p-S6K or p-S6 antibody (clone #4851, Cell Signaling Technology, Danvers, USA) diluent for 1 h. The dilution concentration of the antibody is 1:50. ..

    Concentration Assay:

    Article Title: IL-37d suppresses Rheb-mTORC1 axis independently of TCS2 to alleviate alcoholic liver disease.
    Article Snippet: .. For intracellular cytokine staining, cells were incubated in 100 μl p-S6K or p-S6 antibody (clone #4851, Cell Signaling Technology, Danvers, USA) diluent for 1 h. The dilution concentration of the antibody is 1:50. ..

    Article Title: IL-37d suppresses Rheb-mTORC1 axis independently of TCS2 to alleviate alcoholic liver disease
    Article Snippet: .. For intracellular cytokine staining, cells were incubated in 100 μl p-S6K or p-S6 antibody (clone #4851, Cell Signaling Technology, Danvers, USA) diluent for 1 h. The dilution concentration of the antibody is 1:50. ..

    Immunohistochemical staining:

    Article Title: External auditory canal ectopic atypical meningioma: A case report and brief literature review.
    Article Snippet: The mTOR immunohistochemistry antibody used (#2983, rabbit monoclonal, clone 7C10, Cell Signaling Technology, Denvers, MA, USA) is not designed alone to recognize the phosphorylated form of mTOR. .. Immunohistochemical analysis of mTOR gains value when joined by p-S6 antibody (#5364, rabbit monoclonal, clone D68F8, Cell Signaling Technology, F. Nozzoli et al. ..



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    a Immunoblot analyses were conducted for the indicated proteins in kidney tissues from rtTA and rtTA-Peli1 mice following 12 weeks of doxycycline administration. b Immunohistochemical analysis was carried out for p-S6 <t>(Ser240/244)</t> expression in kidneys at 12 weeks after doxycycline treatment in rtTA and rtTA-Peli1 mice. Scale bars, 50 μm. c Western blotting was used to measure Peli1 and S6K1 protein levels after infection with lentiviral particles containing Peli1 shRNA in HK-2 cells. d Pull-down assays were conducted on 293T cells co-expressing TAP-Peli1 and flag-S6K1; TAP-Peli1 was precipitated with S-beads, and S6K1 co-precipitation was detected by immunoblotting using an anti-S6K1 antibody. e Co-immunoprecipitation was performed for GFP-Peli1 and Flag-S6K1 co-expressed in HK-2 cells. GFP-Peli1 was immunoprecipitated with an anti-GFP antibody, and detection of co-precipitated Flag-S6K1 was done by immunoblotting using the same antibody.
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    a Immunoblot analyses were conducted for the indicated proteins in kidney tissues from rtTA and rtTA-Peli1 mice following 12 weeks of doxycycline administration. b Immunohistochemical analysis was carried out for p-S6 <t>(Ser240/244)</t> expression in kidneys at 12 weeks after doxycycline treatment in rtTA and rtTA-Peli1 mice. Scale bars, 50 μm. c Western blotting was used to measure Peli1 and S6K1 protein levels after infection with lentiviral particles containing Peli1 shRNA in HK-2 cells. d Pull-down assays were conducted on 293T cells co-expressing TAP-Peli1 and flag-S6K1; TAP-Peli1 was precipitated with S-beads, and S6K1 co-precipitation was detected by immunoblotting using an anti-S6K1 antibody. e Co-immunoprecipitation was performed for GFP-Peli1 and Flag-S6K1 co-expressed in HK-2 cells. GFP-Peli1 was immunoprecipitated with an anti-GFP antibody, and detection of co-precipitated Flag-S6K1 was done by immunoblotting using the same antibody.
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    Image Search Results


    a Immunoblot analyses were conducted for the indicated proteins in kidney tissues from rtTA and rtTA-Peli1 mice following 12 weeks of doxycycline administration. b Immunohistochemical analysis was carried out for p-S6 (Ser240/244) expression in kidneys at 12 weeks after doxycycline treatment in rtTA and rtTA-Peli1 mice. Scale bars, 50 μm. c Western blotting was used to measure Peli1 and S6K1 protein levels after infection with lentiviral particles containing Peli1 shRNA in HK-2 cells. d Pull-down assays were conducted on 293T cells co-expressing TAP-Peli1 and flag-S6K1; TAP-Peli1 was precipitated with S-beads, and S6K1 co-precipitation was detected by immunoblotting using an anti-S6K1 antibody. e Co-immunoprecipitation was performed for GFP-Peli1 and Flag-S6K1 co-expressed in HK-2 cells. GFP-Peli1 was immunoprecipitated with an anti-GFP antibody, and detection of co-precipitated Flag-S6K1 was done by immunoblotting using the same antibody.

    Journal: Cell Death & Disease

    Article Title: Pellino1-mTOR/S6K1 signaling axis is a key pathogenesis for the development of polycystic kidney disease

    doi: 10.1038/s41419-026-08479-6

    Figure Lengend Snippet: a Immunoblot analyses were conducted for the indicated proteins in kidney tissues from rtTA and rtTA-Peli1 mice following 12 weeks of doxycycline administration. b Immunohistochemical analysis was carried out for p-S6 (Ser240/244) expression in kidneys at 12 weeks after doxycycline treatment in rtTA and rtTA-Peli1 mice. Scale bars, 50 μm. c Western blotting was used to measure Peli1 and S6K1 protein levels after infection with lentiviral particles containing Peli1 shRNA in HK-2 cells. d Pull-down assays were conducted on 293T cells co-expressing TAP-Peli1 and flag-S6K1; TAP-Peli1 was precipitated with S-beads, and S6K1 co-precipitation was detected by immunoblotting using an anti-S6K1 antibody. e Co-immunoprecipitation was performed for GFP-Peli1 and Flag-S6K1 co-expressed in HK-2 cells. GFP-Peli1 was immunoprecipitated with an anti-GFP antibody, and detection of co-precipitated Flag-S6K1 was done by immunoblotting using the same antibody.

    Article Snippet: For immunohistochemistry, the sections were deparaffinized, treated with citrate buffer for antigen retrieval, stained with anti-P-S6 (Ser240/244) (Cell Signaling, #2215) and anti-Peli1 (Santa Cruz, #sc-271), and incubated using Vectastain Elite ABC kit (Vector Laboratories).

    Techniques: Western Blot, Immunohistochemical staining, Expressing, Infection, shRNA, Immunoprecipitation