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eto  (Baoji Titanium Industry Co Ltd)

 
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    Baoji Titanium Industry Co Ltd eto
    Eto, supplied by Baoji Titanium Industry Co Ltd, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/eto/eto/pmc12748264-78-6-9
    Average 86 stars, based on 1 article reviews
    eto - by Bioz Stars, 2026-09
    86/100 stars

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    Chromatography:

    Article Title: Integrated gut microbiota and metabolomics analysis reveals the antitumor effects of ergosta-4,6,8(14),22-tetraen-3-one purified from the medicinal fungus pholiota adiposa in tumor-bearing mice
    Article Snippet: Structural analysis of ETO was conducted by 1H NMR (600 MHz) and 13C NMR (125 MHz) spectroscopy at the Changchun Institute of Applied Chemistry, Chinese Academy of Sciences ( ). .. Subsequent experiments used chromatography grade 98% ETO purchased from Baoji Chenguang Biotechnology Co. in Shaanxi Province, China. .. Male ICR mice (specific pathogen-free grade, 6–8 weeks old, weight: 20 ± 2 g) were obtained from Liaoning Changsheng Biotechnology Co., Ltd. (Liaoning, China) (Certificate No.: SCXK (Liao) 2023-0001).



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    Inhibition of the mFAO sensitizes muscle to atrophic stress. (a) qRT-PCR analysis of zebrafish larvae treated with DEXA(S) and/or <t>etomoxir</t> <t>(ETO)</t> showing the expression of the atrophy genes fbxo32 and trim63a (DEXA(S) indicates a short-course DEXA treatment. * p < 0.05, t-test, two-tailed, error bar indicates s.d.). (b) Representative fluorescent images of LysoView-stained zebrafish larvae treated with DEXA(S) and/or ETO. Histogram showing quantification of fluorescent intensity (white rectangle indicates the area chosen for the fluorescence quantification. Scale bar represents 1 mm. * p < 0.05, one-way ANOVA and Tukey’s multiple comparison test; error bar indicates s.d.). (c) Representative confocal microscopy images of Alexa488-phalloidin-stained zebrafish larvae treated with DEXA(S) and/or ETO with or without the hormesis treatment (arrows indicate examples of detached muscle fibers). Boxplot shows quantification of larvae with 0, 1–2, 3–15, or >15 detached muscle fibers (* p < 0.05, Chi-square test. Scale bar represents 50 µM).
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    Image Search Results


    Inhibition of the mFAO sensitizes muscle to atrophic stress. (a) qRT-PCR analysis of zebrafish larvae treated with DEXA(S) and/or etomoxir (ETO) showing the expression of the atrophy genes fbxo32 and trim63a (DEXA(S) indicates a short-course DEXA treatment. * p < 0.05, t-test, two-tailed, error bar indicates s.d.). (b) Representative fluorescent images of LysoView-stained zebrafish larvae treated with DEXA(S) and/or ETO. Histogram showing quantification of fluorescent intensity (white rectangle indicates the area chosen for the fluorescence quantification. Scale bar represents 1 mm. * p < 0.05, one-way ANOVA and Tukey’s multiple comparison test; error bar indicates s.d.). (c) Representative confocal microscopy images of Alexa488-phalloidin-stained zebrafish larvae treated with DEXA(S) and/or ETO with or without the hormesis treatment (arrows indicate examples of detached muscle fibers). Boxplot shows quantification of larvae with 0, 1–2, 3–15, or >15 detached muscle fibers (* p < 0.05, Chi-square test. Scale bar represents 50 µM).

    Journal: Frontiers in Cell and Developmental Biology

    Article Title: Sirt1 coordinates the mitochondrial UPR and myocellular proteostasis to preserve muscle integrity during muscle atrophy in zebrafish

    doi: 10.3389/fcell.2026.1761278

    Figure Lengend Snippet: Inhibition of the mFAO sensitizes muscle to atrophic stress. (a) qRT-PCR analysis of zebrafish larvae treated with DEXA(S) and/or etomoxir (ETO) showing the expression of the atrophy genes fbxo32 and trim63a (DEXA(S) indicates a short-course DEXA treatment. * p < 0.05, t-test, two-tailed, error bar indicates s.d.). (b) Representative fluorescent images of LysoView-stained zebrafish larvae treated with DEXA(S) and/or ETO. Histogram showing quantification of fluorescent intensity (white rectangle indicates the area chosen for the fluorescence quantification. Scale bar represents 1 mm. * p < 0.05, one-way ANOVA and Tukey’s multiple comparison test; error bar indicates s.d.). (c) Representative confocal microscopy images of Alexa488-phalloidin-stained zebrafish larvae treated with DEXA(S) and/or ETO with or without the hormesis treatment (arrows indicate examples of detached muscle fibers). Boxplot shows quantification of larvae with 0, 1–2, 3–15, or >15 detached muscle fibers (* p < 0.05, Chi-square test. Scale bar represents 50 µM).

    Article Snippet: To block Cpt1 activity, larval zebrafish at 4 dpf were treated with 10 μM etomoxir (ETO) (Selleckchem) with or without DEXA for 18 h–20 h. To suppress autophagy, 5 mM chloroquine (Sigma) was added to the larval zebrafish medium for 1-h incubation.

    Techniques: Inhibition, Quantitative RT-PCR, Expressing, Two Tailed Test, Staining, Fluorescence, Comparison, Confocal Microscopy