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. 2020 Mar 30;21:265. doi: 10.1186/s12864-020-6684-z

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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 — Inhibition of proliferation of HepG2 cells by the three partially purified fractions from the MEF 134 crude extracts. a Representative light microscopy images of HepG2 cells treated with the MEF 134 fractions. The dose of each fraction used for the assay is indicated in percentages (w/v). b-d Quantification of the anti-proliferative effect of the fractions. The fractions used for the assay were FD K1V1V1 (V1), FD K1V5V3 (V3) and FD K2V3V5 (V5). All measurements were performed in biological duplicates. All three fractions had antifungal activity against S. cerevisiae only