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p p53 ser 15 rabbit polyclonal  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc p p53 ser 15 rabbit polyclonal
    3BP deactivates Akt and induces <t>p53</t> degradation in U118 cells. Cells were subjected to 3BP treatments for 2 h and analysed by Western blotting for phosphorylated and total Akt or p53 proteins. Actin is a loading control. Each membrane was probed sequentially with phosphorylated and total protein antibodies, followed by actin antibody. Representative blots are shown. Data are the mean ± SD of three independent experiments (∗p < 0.05; ∗∗p < 0.01). The full blot images are available as Supplementary material-original blottings.
    P P53 Ser 15 Rabbit Polyclonal, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 93/100, based on 158 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/p p53 ser 15 rabbit polyclonal/product/Cell Signaling Technology Inc
    Average 93 stars, based on 158 article reviews
    p p53 ser 15 rabbit polyclonal - by Bioz Stars, 2026-03
    93/100 stars

    Images

    1) Product Images from "The efficacy of the anticancer 3-bromopyruvate is potentiated by antimycin and menadione by unbalancing mitochondrial ROS production and disposal in U118 glioblastoma cells"

    Article Title: The efficacy of the anticancer 3-bromopyruvate is potentiated by antimycin and menadione by unbalancing mitochondrial ROS production and disposal in U118 glioblastoma cells

    Journal: Heliyon

    doi: 10.1016/j.heliyon.2020.e05741

    3BP deactivates Akt and induces p53 degradation in U118 cells. Cells were subjected to 3BP treatments for 2 h and analysed by Western blotting for phosphorylated and total Akt or p53 proteins. Actin is a loading control. Each membrane was probed sequentially with phosphorylated and total protein antibodies, followed by actin antibody. Representative blots are shown. Data are the mean ± SD of three independent experiments (∗p < 0.05; ∗∗p < 0.01). The full blot images are available as Supplementary material-original blottings.
    Figure Legend Snippet: 3BP deactivates Akt and induces p53 degradation in U118 cells. Cells were subjected to 3BP treatments for 2 h and analysed by Western blotting for phosphorylated and total Akt or p53 proteins. Actin is a loading control. Each membrane was probed sequentially with phosphorylated and total protein antibodies, followed by actin antibody. Representative blots are shown. Data are the mean ± SD of three independent experiments (∗p < 0.05; ∗∗p < 0.01). The full blot images are available as Supplementary material-original blottings.

    Techniques Used: Western Blot, Control, Membrane



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    3BP deactivates Akt and induces <t>p53</t> degradation in U118 cells. Cells were subjected to 3BP treatments for 2 h and analysed by Western blotting for phosphorylated and total Akt or p53 proteins. Actin is a loading control. Each membrane was probed sequentially with phosphorylated and total protein antibodies, followed by actin antibody. Representative blots are shown. Data are the mean ± SD of three independent experiments (∗p < 0.05; ∗∗p < 0.01). The full blot images are available as Supplementary material-original blottings.
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    Image Search Results


    3BP deactivates Akt and induces p53 degradation in U118 cells. Cells were subjected to 3BP treatments for 2 h and analysed by Western blotting for phosphorylated and total Akt or p53 proteins. Actin is a loading control. Each membrane was probed sequentially with phosphorylated and total protein antibodies, followed by actin antibody. Representative blots are shown. Data are the mean ± SD of three independent experiments (∗p < 0.05; ∗∗p < 0.01). The full blot images are available as Supplementary material-original blottings.

    Journal: Heliyon

    Article Title: The efficacy of the anticancer 3-bromopyruvate is potentiated by antimycin and menadione by unbalancing mitochondrial ROS production and disposal in U118 glioblastoma cells

    doi: 10.1016/j.heliyon.2020.e05741

    Figure Lengend Snippet: 3BP deactivates Akt and induces p53 degradation in U118 cells. Cells were subjected to 3BP treatments for 2 h and analysed by Western blotting for phosphorylated and total Akt or p53 proteins. Actin is a loading control. Each membrane was probed sequentially with phosphorylated and total protein antibodies, followed by actin antibody. Representative blots are shown. Data are the mean ± SD of three independent experiments (∗p < 0.05; ∗∗p < 0.01). The full blot images are available as Supplementary material-original blottings.

    Article Snippet: Akt rabbit polyclonal, p-Akt (Ser-473) rabbit monoclonal, JNK rabbit monoclonal, p-JNK (Thr183/Tyr185) rabbit monoclonal, p44/42 MAPK (ERK1/2) rabbit monoclonal, p-ERK1/2 (Thr202/Tyr204) rabbit monoclonal, p38 MAPK rabbit polyclonal, p-p38 (Thr180/Tyr182) rabbit monoclonal, p-p53 (Ser-15) rabbit polyclonal, caspase-3 rabbit polyclonal, and caspase-9 rabbit polyclonal antibodies were from Cell Signaling Technology.

    Techniques: Western Blot, Control, Membrane