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. 2014 Feb 15;4(5):460–474. doi: 10.7150/thno.8077

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© Ivyspring International Publisher. This is an open-access article distributed under the terms of the Creative Commons License (http://creativecommons.org/licenses/by-nc-nd/3.0/). Reproduction is permitted for personal, noncommercial use, provided that the article is in whole, unmodified, and properly cited.

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A. FACS analysis of MDA-MB-231 stable cells expressing HSV1-sr39TK, NTR and HSV1-sr39TK-NTR fusion proteins treated with various concentrations and combinations of GCV, CB1954 for 3 days and stained with propidium iodide (PI). Percentage of live and dead cells are labeled. B. FACS analysis of MDA-MB-231 HSV1-sr39TK, NTR and HSV1-sr39TK-NTR stable cells treated with a combination of 1 μg GCV and 10 μM CB1954 and assayed for five consecutive days. Percentage of live and dead cells are labeled in each sample panel.

A. FACS analysis of MDA-MB-231 stable cells expressing HSV1-sr39TK, NTR and HSV1-sr39TK-NTR fusion proteins treated with various concentrations and combinations of GCV, CB1954 for 3 days and stained with propidium iodide (PI). Percentage of live and dead cells are labeled. B. FACS analysis of MDA-MB-231 HSV1-sr39TK, NTR and HSV1-sr39TK-NTR stable cells treated with a combination of 1 μg GCV and 10 μM CB1954 and assayed for five consecutive days. Percentage of live and dead cells are labeled in each sample panel.