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. 2018 Jan 15;8:737. doi: 10.1038/s41598-017-18658-3

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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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Myotubes contain more mitochondria-specific proteins than myoblasts. Proteins were extracted from myoblasts and myotubes and characterised by immunoblot according to Fig. 2. Only pre-respirometry samples are shown. (a) Abundance normalised to protein loaded of mitochondrial abundance markers (CS and HSP60), respiratory chain complex enzymes (UQCRC2, MTCO1 and ATP5), β-oxidation enzymes (HADHA and MCAD), and RPS6 as a housekeeping protein (b) Abundance normalised to CS. Only vehicle-treated cells are shown. All values were standardised to myoblasts protein abundances. Two-sided t-tests, *p < 0.05, **p < 0.01, ***p < 0.001. n = 3–4, mean ± SD. Due to missing CS values, less data points could be included for (b) than for (a).