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. 2021 Apr 9;7:73. doi: 10.1038/s41420-021-00463-7

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© The Author(s) 2021

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, B Myotube area (%) of CPM cells transfected with pcDNA3.1-lncRNA-FKBP1C, pcDNA3.1, si-ASO-lncRNA-FKBP1C or si-NC. C MyHC Immunofluorescence staining of CPM cells. D The relative expression of lncRNA-FKBP1C during CPM differentiation. E, F The relative expression of MyoD, MyoG, and MyHC. G, H The protein expression of MyHC, MyoD, MyoG were determined by Western blotting in CPM cells. Results are shown as mean ± S.E.M. and the data are representative of at least three independent assays. Independent sample t-test was used to analyze the statistical differences between groups (*P < 0.05, **P < 0.01, ***P < 0.001).