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. 2020 Jul 6;20:209. doi: 10.1186/s12906-020-02965-w

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© The Author(s) 2020

Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

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Fig. 4 — Myricetin induced the apoptosis of HCT116 and SW620 cells. a Apoptosis was determined by flow cytometry, and b the percentage of cell viability was quantified with a histogram (the early and late apoptotic cells are also considered). c Bax and Bcl-2 were detected by Western blotting with β-actin as the loading control. d Quantification of the Western blotting results as a histogram. The experiment was repeated three times (*p < 0.05, **p < 0.01, and ***p < 0.001 vs. control)