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. 2018 Mar 21;8:4989. doi: 10.1038/s41598-018-22740-9

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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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Purification of Cyt1Aa-hybrid proteins expressed in B. thuringiensis 407^- strain. Panel A, purified trypsin activated toxins resolved in SDS-PAGE 15% acrylamide stained with Coomassie blue. Panel B, analysis of hybrid Cyt1Aa protoxins by western blot assays using anti-Cyt1Aa polyclonal specific antibody. Panel C, analysis of hybrid Cyt1Aa activated toxins by western blot assays using anti-Cyt1Aa polyclonal specific antibody. Page ruler plus pre-stained protein ladder in panels B and C are shown as separate images.