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. 2022 Aug 17;13(8):716. doi: 10.1038/s41419-022-05160-6

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© The Author(s) 2022

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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Fig. 3 — A Dystrophin levels tended to be reduced three weeks after DDp53 electroporation. B The membrane-damage activated protein dysferlin was increased with DDp53 electroporation. C Similarly, annexin A2 levels increased with DDp53. D Myosin heavy chain type I (slow isoform/MHCs) protein levels was elevated in the DDp53 electroporated muscle compared to the control leg. E Pro-collagen (proCol1α1) synthesis was increased in the DDp53 leg compared to the control leg. F Muscle LIM (mLIM) protein levels were unchanged with DDp53. Individual data points represent each animal. Squares represent the leg that was electroporated with DDp53, circles the contralateral control leg of the same animals. Western blot images show three representative bands from each condition. Both representative pictures stem from the same membrane and exposure time. All western blots were normalized to total protein per lane. Original, unaltered images of all membranes and the gels that they were normalized to can be found in the data supplement. n = 12, * indicates a p-value of <0.05 and ** indicates a p-value of <0.01.