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garcinol  (BOC Sciences)


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    Structured Review

    BOC Sciences garcinol
    Acetylation by GCN5b stabilizes TgGSK. (A) Plot of TgGSK immunoprecipitation data. More significant interactors are toward the upper right of the plot. Points in red are members of the GCN5b complex. (B) IFA of <t>non-dividing</t> <t>GSK.3xHA</t> parasites treated with 0, 2, or 4 µM <t>garcinol</t> for 18 hours. Staining was done for IMC3, HA, and DAPI to visualize IMC, TgGSK, and nuclear material, respectively. (C) Western blot analysis of TgGSK protein levels after 18 hours of garcinol treatment. The cytosolic protein aldolase was used as a control.
    Garcinol, supplied by BOC Sciences, used in various techniques. Bioz Stars score: 93/100, based on 2 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/garcinol/product/BOC Sciences
    Average 93 stars, based on 2 article reviews
    garcinol - by Bioz Stars, 2026-02
    93/100 stars

    Images

    1) Product Images from "The essential kinase TgGSK regulates centrosome segregation and endodyogeny in Toxoplasma gondii"

    Article Title: The essential kinase TgGSK regulates centrosome segregation and endodyogeny in Toxoplasma gondii

    Journal: mSphere

    doi: 10.1128/msphere.00111-25

    Acetylation by GCN5b stabilizes TgGSK. (A) Plot of TgGSK immunoprecipitation data. More significant interactors are toward the upper right of the plot. Points in red are members of the GCN5b complex. (B) IFA of non-dividing GSK.3xHA parasites treated with 0, 2, or 4 µM garcinol for 18 hours. Staining was done for IMC3, HA, and DAPI to visualize IMC, TgGSK, and nuclear material, respectively. (C) Western blot analysis of TgGSK protein levels after 18 hours of garcinol treatment. The cytosolic protein aldolase was used as a control.
    Figure Legend Snippet: Acetylation by GCN5b stabilizes TgGSK. (A) Plot of TgGSK immunoprecipitation data. More significant interactors are toward the upper right of the plot. Points in red are members of the GCN5b complex. (B) IFA of non-dividing GSK.3xHA parasites treated with 0, 2, or 4 µM garcinol for 18 hours. Staining was done for IMC3, HA, and DAPI to visualize IMC, TgGSK, and nuclear material, respectively. (C) Western blot analysis of TgGSK protein levels after 18 hours of garcinol treatment. The cytosolic protein aldolase was used as a control.

    Techniques Used: Immunoprecipitation, Staining, Western Blot, Control



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    Acetylation by GCN5b stabilizes TgGSK. (A) Plot of TgGSK immunoprecipitation data. More significant interactors are toward the upper right of the plot. Points in red are members of the GCN5b complex. (B) IFA of <t>non-dividing</t> <t>GSK.3xHA</t> parasites treated with 0, 2, or 4 µM <t>garcinol</t> for 18 hours. Staining was done for IMC3, HA, and DAPI to visualize IMC, TgGSK, and nuclear material, respectively. (C) Western blot analysis of TgGSK protein levels after 18 hours of garcinol treatment. The cytosolic protein aldolase was used as a control.
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    Acetylation by GCN5b stabilizes TgGSK. (A) Plot of TgGSK immunoprecipitation data. More significant interactors are toward the upper right of the plot. Points in red are members of the GCN5b complex. (B) IFA of <t>non-dividing</t> <t>GSK.3xHA</t> parasites treated with 0, 2, or 4 µM <t>garcinol</t> for 18 hours. Staining was done for IMC3, HA, and DAPI to visualize IMC, TgGSK, and nuclear material, respectively. (C) Western blot analysis of TgGSK protein levels after 18 hours of garcinol treatment. The cytosolic protein aldolase was used as a control.
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    Acetylation by GCN5b stabilizes TgGSK. (A) Plot of TgGSK immunoprecipitation data. More significant interactors are toward the upper right of the plot. Points in red are members of the GCN5b complex. (B) IFA of <t>non-dividing</t> <t>GSK.3xHA</t> parasites treated with 0, 2, or 4 µM <t>garcinol</t> for 18 hours. Staining was done for IMC3, HA, and DAPI to visualize IMC, TgGSK, and nuclear material, respectively. (C) Western blot analysis of TgGSK protein levels after 18 hours of garcinol treatment. The cytosolic protein aldolase was used as a control.
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    Acetylation by GCN5b stabilizes TgGSK. (A) Plot of TgGSK immunoprecipitation data. More significant interactors are toward the upper right of the plot. Points in red are members of the GCN5b complex. (B) IFA of <t>non-dividing</t> <t>GSK.3xHA</t> parasites treated with 0, 2, or 4 µM <t>garcinol</t> for 18 hours. Staining was done for IMC3, HA, and DAPI to visualize IMC, TgGSK, and nuclear material, respectively. (C) Western blot analysis of TgGSK protein levels after 18 hours of garcinol treatment. The cytosolic protein aldolase was used as a control.
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    Image Search Results


    Acetylation by GCN5b stabilizes TgGSK. (A) Plot of TgGSK immunoprecipitation data. More significant interactors are toward the upper right of the plot. Points in red are members of the GCN5b complex. (B) IFA of non-dividing GSK.3xHA parasites treated with 0, 2, or 4 µM garcinol for 18 hours. Staining was done for IMC3, HA, and DAPI to visualize IMC, TgGSK, and nuclear material, respectively. (C) Western blot analysis of TgGSK protein levels after 18 hours of garcinol treatment. The cytosolic protein aldolase was used as a control.

    Journal: mSphere

    Article Title: The essential kinase TgGSK regulates centrosome segregation and endodyogeny in Toxoplasma gondii

    doi: 10.1128/msphere.00111-25

    Figure Lengend Snippet: Acetylation by GCN5b stabilizes TgGSK. (A) Plot of TgGSK immunoprecipitation data. More significant interactors are toward the upper right of the plot. Points in red are members of the GCN5b complex. (B) IFA of non-dividing GSK.3xHA parasites treated with 0, 2, or 4 µM garcinol for 18 hours. Staining was done for IMC3, HA, and DAPI to visualize IMC, TgGSK, and nuclear material, respectively. (C) Western blot analysis of TgGSK protein levels after 18 hours of garcinol treatment. The cytosolic protein aldolase was used as a control.

    Article Snippet: GSK.3xHA parasites were seeded simultaneously with 2 or 4 μM Garcinol (BOC Sciences) in 1% serum media for 18 hours.

    Techniques: Immunoprecipitation, Staining, Western Blot, Control