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. 2018 Sep 14;8:13857. doi: 10.1038/s41598-018-32216-5

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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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Western blot analysis against anti-MEK1/2 and ERK1/2. ATPβ antibody was detected as a loading control. Cell lysates cultivated under 0, 0.05, 0.1, and 0.15 M concentrations of NaCl were analyzed with phospho-specific antibodies to measure the MEK1/2 and ERK1/2 activities. Full-length blots are presented in Supplementary Fig. S6. Relative expression of proteins is represented as mean ± SD (n = 3). Significant differences were determined by Student’s t-test and indicated by asterisks (*P < 0.05, **P < 0.01, ***P < 0.001).