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. 2018 Jan 15;8:705. doi: 10.1038/s41598-017-17940-8

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© The Author(s) 2018

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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Purity of UVDE-TAT, UVDE-NLS-TAT, and cv-pdg-NLS. The purity of the DNA repair enzymes was assessed by Coomassie staining of proteins following electrophoretic separation through a denaturing 15% polyacrylamide gel. A total of 5 µg of UVDE-TAT, UVDE-NLS-TAT, and cv-pdg-NLS were run in lanes as indicated. Pre-stained markers were run in the left lane, with molecular weights given.