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. 2017 Nov 1;7:14799. doi: 10.1038/s41598-017-14558-8

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© The Author(s) 2017

Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.

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Subcellular localisation of CAV VP2 and Apoptin in CHO-K1 cells. CHO-K1 cells were transfected with pmCherry-C1 and pmCherry-VP2 (A) or pEGFP-C2 and pEGFP-VP3 (B), respectively. At 48 hrs post-transfection, the cells were fixed and stained with DAPI as a nuclear indicator, followed by confocal microscopy. The distribution of red fluorescence in CHO-K1 cells indicated the subcellular localisation of overexpressed mCherry or mCherry-VP2; green fluorescent indicated the localisation of EGFP or EGFP-Apoptin. The localisation of VP2 and Apoptin in CHO-K1 cells was determined after comparing the merged images between the sole fluorescent protein and fluorescent protein-fused protein.