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stat3 phosphorylation inhibitor stattic  (MedChemExpress)


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    Structured Review

    MedChemExpress stat3 phosphorylation inhibitor stattic
    Stat3 Phosphorylation Inhibitor Stattic, supplied by MedChemExpress, used in various techniques. Bioz Stars score: 98/100, based on 367 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/stat3 phosphorylation inhibitor stattic/product/MedChemExpress
    Average 98 stars, based on 367 article reviews
    stat3 phosphorylation inhibitor stattic - by Bioz Stars, 2026-02
    98/100 stars

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    Effects of minocycline on <t>STAT3</t> activation and GLS1 expression in LTA-induced microglial cells. ( A , B ) The expression levels of p-STAT3, STAT3, and GLS1 in the BV2 and N9 cells were analyzed via Western blot analysis. ( C , D ) The quantification of the expression levels of p-STAT3/STAT3 and GLS1 in BV2 and N9 cells. The data were normalized according to GAPDH. The mean ± SEM of three separate experiments is represented for all data that have error bars. Compared to the control group, * p < 0.05; ** p < 0.01; *** p < 0.001. Compared to the LTA group, # p < 0.05; ## p < 0.01; ### p < 0.001. Control, saline-treated group; LTA, cells pretreated with saline and then stimulated with LTA; Mino100 + LTA, cells pretreated with 100 μmol/L minocycline and then stimulated with LTA; Mino200 + LTA, cells pretreated with 200 μmol/L minocycline and then stimulated with LTA.
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    Effects of minocycline on <t>STAT3</t> activation and GLS1 expression in LTA-induced microglial cells. ( A , B ) The expression levels of p-STAT3, STAT3, and GLS1 in the BV2 and N9 cells were analyzed via Western blot analysis. ( C , D ) The quantification of the expression levels of p-STAT3/STAT3 and GLS1 in BV2 and N9 cells. The data were normalized according to GAPDH. The mean ± SEM of three separate experiments is represented for all data that have error bars. Compared to the control group, * p < 0.05; ** p < 0.01; *** p < 0.001. Compared to the LTA group, # p < 0.05; ## p < 0.01; ### p < 0.001. Control, saline-treated group; LTA, cells pretreated with saline and then stimulated with LTA; Mino100 + LTA, cells pretreated with 100 μmol/L minocycline and then stimulated with LTA; Mino200 + LTA, cells pretreated with 200 μmol/L minocycline and then stimulated with LTA.
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    Effects of minocycline on <t>STAT3</t> activation and GLS1 expression in LTA-induced microglial cells. ( A , B ) The expression levels of p-STAT3, STAT3, and GLS1 in the BV2 and N9 cells were analyzed via Western blot analysis. ( C , D ) The quantification of the expression levels of p-STAT3/STAT3 and GLS1 in BV2 and N9 cells. The data were normalized according to GAPDH. The mean ± SEM of three separate experiments is represented for all data that have error bars. Compared to the control group, * p < 0.05; ** p < 0.01; *** p < 0.001. Compared to the LTA group, # p < 0.05; ## p < 0.01; ### p < 0.001. Control, saline-treated group; LTA, cells pretreated with saline and then stimulated with LTA; Mino100 + LTA, cells pretreated with 100 μmol/L minocycline and then stimulated with LTA; Mino200 + LTA, cells pretreated with 200 μmol/L minocycline and then stimulated with LTA.
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    Effects of minocycline on <t>STAT3</t> activation and GLS1 expression in LTA-induced microglial cells. ( A , B ) The expression levels of p-STAT3, STAT3, and GLS1 in the BV2 and N9 cells were analyzed via Western blot analysis. ( C , D ) The quantification of the expression levels of p-STAT3/STAT3 and GLS1 in BV2 and N9 cells. The data were normalized according to GAPDH. The mean ± SEM of three separate experiments is represented for all data that have error bars. Compared to the control group, * p < 0.05; ** p < 0.01; *** p < 0.001. Compared to the LTA group, # p < 0.05; ## p < 0.01; ### p < 0.001. Control, saline-treated group; LTA, cells pretreated with saline and then stimulated with LTA; Mino100 + LTA, cells pretreated with 100 μmol/L minocycline and then stimulated with LTA; Mino200 + LTA, cells pretreated with 200 μmol/L minocycline and then stimulated with LTA.
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    Millipore stattic hydrochloride (>95%) which is a potent stat3 inhibitor and inhibits stat3 phosphorylation (at y705 and s727)
    TTFields combined sorafenib inhibits the phosphorylation of <t>STAT3</t> and AKT and then suppresses STAT3 transcription activity. (A) Western blot analysis of HCT116 cell lysates, following 24 h cell culture in the presence of LY294002 (10 µM) or Stattic (10 µM). (B) Prior to being treated for 36 hours before dual-luciferase assay, SW480 and HCT116 cells were transfected with internal control pRL-SV40 Renilla luciferase construct and nonresponsive control reporter pLucTK/pLucTKS3. **P<0.01. TTF, tumor-treating fields; S + T, sorafenib + tumor-treating fields; S, sorafenib; TTFields, tumor-treating fields.
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    Effects of minocycline on STAT3 activation and GLS1 expression in LTA-induced microglial cells. ( A , B ) The expression levels of p-STAT3, STAT3, and GLS1 in the BV2 and N9 cells were analyzed via Western blot analysis. ( C , D ) The quantification of the expression levels of p-STAT3/STAT3 and GLS1 in BV2 and N9 cells. The data were normalized according to GAPDH. The mean ± SEM of three separate experiments is represented for all data that have error bars. Compared to the control group, * p < 0.05; ** p < 0.01; *** p < 0.001. Compared to the LTA group, # p < 0.05; ## p < 0.01; ### p < 0.001. Control, saline-treated group; LTA, cells pretreated with saline and then stimulated with LTA; Mino100 + LTA, cells pretreated with 100 μmol/L minocycline and then stimulated with LTA; Mino200 + LTA, cells pretreated with 200 μmol/L minocycline and then stimulated with LTA.

    Journal: Brain Sciences

    Article Title: Minocycline Ameliorates Staphylococcus aureus -Induced Neuroinflammation and Anxiety-like Behaviors by Regulating the TLR2 and STAT3 Pathways in Microglia

    doi: 10.3390/brainsci15020128

    Figure Lengend Snippet: Effects of minocycline on STAT3 activation and GLS1 expression in LTA-induced microglial cells. ( A , B ) The expression levels of p-STAT3, STAT3, and GLS1 in the BV2 and N9 cells were analyzed via Western blot analysis. ( C , D ) The quantification of the expression levels of p-STAT3/STAT3 and GLS1 in BV2 and N9 cells. The data were normalized according to GAPDH. The mean ± SEM of three separate experiments is represented for all data that have error bars. Compared to the control group, * p < 0.05; ** p < 0.01; *** p < 0.001. Compared to the LTA group, # p < 0.05; ## p < 0.01; ### p < 0.001. Control, saline-treated group; LTA, cells pretreated with saline and then stimulated with LTA; Mino100 + LTA, cells pretreated with 100 μmol/L minocycline and then stimulated with LTA; Mino200 + LTA, cells pretreated with 200 μmol/L minocycline and then stimulated with LTA.

    Article Snippet: The STAT3 phosphorylation (at Y705 and S727) inhibitor Stattic was purchased from MCE (Princeton, NJ, USA).

    Techniques: Activation Assay, Expressing, Western Blot, Control, Saline

    The inhibition of p-STAT3 reduces the proinflammatory cytokines and GLS1 levels in LTA-induced microglial cells. ( A , B ) The TNF-α, IL-6, and IL-10 secreted by the BV2 and N9 cells were assessed via ELISA. ( C , D ) The expression levels of TLR2, TNF-α, IL-6, GLS1, p-STAT3, and STAT3 in the BV2 and N9 cells were analyzed via Western blot analysis. ( E , F ) The quantification of the expression levels of p-STAT3/STAT3, TLR2, TNF-α, IL-6, and GLS1 in the BV2 and N9 cells. The data were normalized according to GAPDH. The mean ± SEM of three separate experiments is represented for all data that have error bars. Compared to the control group, * p < 0.05; ** p < 0.01; *** p < 0.001. Compared to the LTA group, # p < 0.05; ## p < 0.01; ### p < 0.001. Control, saline-treated group; LTA, cells pretreated with saline and then stimulated with LTA; Stattic, cells pretreated with 10 μmol/L Stattic and then treated with saline; Stattic + LTA, cells pretreated with 10 μmol/L Stattic and then stimulated with LTA.

    Journal: Brain Sciences

    Article Title: Minocycline Ameliorates Staphylococcus aureus -Induced Neuroinflammation and Anxiety-like Behaviors by Regulating the TLR2 and STAT3 Pathways in Microglia

    doi: 10.3390/brainsci15020128

    Figure Lengend Snippet: The inhibition of p-STAT3 reduces the proinflammatory cytokines and GLS1 levels in LTA-induced microglial cells. ( A , B ) The TNF-α, IL-6, and IL-10 secreted by the BV2 and N9 cells were assessed via ELISA. ( C , D ) The expression levels of TLR2, TNF-α, IL-6, GLS1, p-STAT3, and STAT3 in the BV2 and N9 cells were analyzed via Western blot analysis. ( E , F ) The quantification of the expression levels of p-STAT3/STAT3, TLR2, TNF-α, IL-6, and GLS1 in the BV2 and N9 cells. The data were normalized according to GAPDH. The mean ± SEM of three separate experiments is represented for all data that have error bars. Compared to the control group, * p < 0.05; ** p < 0.01; *** p < 0.001. Compared to the LTA group, # p < 0.05; ## p < 0.01; ### p < 0.001. Control, saline-treated group; LTA, cells pretreated with saline and then stimulated with LTA; Stattic, cells pretreated with 10 μmol/L Stattic and then treated with saline; Stattic + LTA, cells pretreated with 10 μmol/L Stattic and then stimulated with LTA.

    Article Snippet: The STAT3 phosphorylation (at Y705 and S727) inhibitor Stattic was purchased from MCE (Princeton, NJ, USA).

    Techniques: Inhibition, Enzyme-linked Immunosorbent Assay, Expressing, Western Blot, Control, Saline

    Effects of minocycline on S. aureus -induced neuroinflammation in vivo. ( A ) The GLS1, p-STAT3, and STAT3 expression levels in the mPFC of two representative mice were analyzed via Western blot analysis. ( B ) The expression levels of p-STAT3/STAT3 and GLS1 in the mPFC were quantified. The data were normalized according to GAPDH. Data are presented as mean ± SEM, n = 4. ( C ) The TLR2, TNF-α, and IL-6 protein expression levels in the mPFC of two representative mice were analyzed via Western blot analysis. ( D ) The expression levels of TLR2, TNF-α, and IL-6 in the mPFC were quantified. The data were normalized according to GAPDH. Data are presented as mean ± SEM, n = 4. ( E ) Schematic diagram showing the mPFC area (red box) of the mice analyzed via immunofluorescent staining. ( F ) Representative fluorescence micrographs showing the number of microglia in the mPFC in the various groups (IBA1, red; DAPI, blue); scale bar = 100 μm. ( G ) A quantitative analysis of the number of IBA1 + cells in the mPFC. Data are presented as mean ± SEM, n = 3. USA300 group compared to the control group, * p < 0.05. Mino + USA300 group compared to the USA300 group, # p < 0.05; ## p < 0.01. Control, saline-treated group; Mino, mice pretreated with minocycline and then challenged with the saline group; USA300, mice pretreated with saline and then challenged with the USA300 group; Mino + USA300, mice pretreated with minocycline and then challenged with the USA300 group.

    Journal: Brain Sciences

    Article Title: Minocycline Ameliorates Staphylococcus aureus -Induced Neuroinflammation and Anxiety-like Behaviors by Regulating the TLR2 and STAT3 Pathways in Microglia

    doi: 10.3390/brainsci15020128

    Figure Lengend Snippet: Effects of minocycline on S. aureus -induced neuroinflammation in vivo. ( A ) The GLS1, p-STAT3, and STAT3 expression levels in the mPFC of two representative mice were analyzed via Western blot analysis. ( B ) The expression levels of p-STAT3/STAT3 and GLS1 in the mPFC were quantified. The data were normalized according to GAPDH. Data are presented as mean ± SEM, n = 4. ( C ) The TLR2, TNF-α, and IL-6 protein expression levels in the mPFC of two representative mice were analyzed via Western blot analysis. ( D ) The expression levels of TLR2, TNF-α, and IL-6 in the mPFC were quantified. The data were normalized according to GAPDH. Data are presented as mean ± SEM, n = 4. ( E ) Schematic diagram showing the mPFC area (red box) of the mice analyzed via immunofluorescent staining. ( F ) Representative fluorescence micrographs showing the number of microglia in the mPFC in the various groups (IBA1, red; DAPI, blue); scale bar = 100 μm. ( G ) A quantitative analysis of the number of IBA1 + cells in the mPFC. Data are presented as mean ± SEM, n = 3. USA300 group compared to the control group, * p < 0.05. Mino + USA300 group compared to the USA300 group, # p < 0.05; ## p < 0.01. Control, saline-treated group; Mino, mice pretreated with minocycline and then challenged with the saline group; USA300, mice pretreated with saline and then challenged with the USA300 group; Mino + USA300, mice pretreated with minocycline and then challenged with the USA300 group.

    Article Snippet: The STAT3 phosphorylation (at Y705 and S727) inhibitor Stattic was purchased from MCE (Princeton, NJ, USA).

    Techniques: In Vivo, Expressing, Western Blot, Staining, Fluorescence, Control, Saline

    TTFields combined sorafenib inhibits the phosphorylation of STAT3 and AKT and then suppresses STAT3 transcription activity. (A) Western blot analysis of HCT116 cell lysates, following 24 h cell culture in the presence of LY294002 (10 µM) or Stattic (10 µM). (B) Prior to being treated for 36 hours before dual-luciferase assay, SW480 and HCT116 cells were transfected with internal control pRL-SV40 Renilla luciferase construct and nonresponsive control reporter pLucTK/pLucTKS3. **P<0.01. TTF, tumor-treating fields; S + T, sorafenib + tumor-treating fields; S, sorafenib; TTFields, tumor-treating fields.

    Journal: Translational Cancer Research

    Article Title: Tumor-treating fields in combination with sorafenib curtails the growth of colorectal carcinoma by inactivating AKT/STAT3 signaling

    doi: 10.21037/tcr-21-1853

    Figure Lengend Snippet: TTFields combined sorafenib inhibits the phosphorylation of STAT3 and AKT and then suppresses STAT3 transcription activity. (A) Western blot analysis of HCT116 cell lysates, following 24 h cell culture in the presence of LY294002 (10 µM) or Stattic (10 µM). (B) Prior to being treated for 36 hours before dual-luciferase assay, SW480 and HCT116 cells were transfected with internal control pRL-SV40 Renilla luciferase construct and nonresponsive control reporter pLucTK/pLucTKS3. **P<0.01. TTF, tumor-treating fields; S + T, sorafenib + tumor-treating fields; S, sorafenib; TTFields, tumor-treating fields.

    Article Snippet: Stattic hydrochloride (>95%) which is a potent STAT3 inhibitor and inhibits STAT3 phosphorylation (at Y705 and S727) was purchased from Sigma-Aldrich (19983-44-9).

    Techniques: Activity Assay, Western Blot, Cell Culture, Luciferase, Transfection, Control, Construct