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. 2020 Oct 29;25(21):5016. doi: 10.3390/molecules25215016

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© 2020 by the authors.

Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).

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Apoptosis induction in NCI-H929 cell lines. Annexin V/PI assay of NCI-H929 cells incubated with 0.5, 1, 2, 4 × IC₅₀ of chloroform fractions of (A)-T. vulgaris (TCF) and (B)-A. lappa (ACF) for 48 and 72 h. Morphology of NCI-H929 cell was noticed under fluorescence microscope by using 4′,6-diamidino-2-phenylindole (DAPI) stain. Yellow arrows referred to apoptotic features were observed in A-TCF and B-ACF treated cells vs. untreated cells. Control: NCI-H929 cell without treatment.

Apoptosis induction in NCI-H929 cell lines. Annexin V/PI assay of NCI-H929 cells incubated with 0.5, 1, 2, 4 × IC₅₀ of chloroform fractions of (A)-T. vulgaris (TCF) and (B)-A. lappa (ACF) for 48 and 72 h. Morphology of NCI-H929 cell was noticed under fluorescence microscope by using 4′,6-diamidino-2-phenylindole (DAPI) stain. Yellow arrows referred to apoptotic features were observed in A-TCF and B-ACF treated cells vs. untreated cells. Control: NCI-H929 cell without treatment.