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. 2015 Jun 27;32(6):605–622. doi: 10.1007/s10585-015-9731-4

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© The Author(s) 2015

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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.

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Fig. 3 — a The 2-DE gel showing the different spot intensities between OS-RC-2 and OS-RC-2-BM5. Among these altered proteins, 25 protein spots (P < 0.05) were noticeably down-regulated in the OS-RC-2-BM5 group (middle panel) and 75 protein spots (P < 0.05) were significantly up-regulated in the OS-RC-2-BM5 group on the right panel. b Results of quantitative Western blotting experiments performed for 26 proteins (change fold <0.5 and >1.9). The magnified images of protein spots from the 2-DE gels were shown on the upper part of each panel and the Western blot replicate results list below. The line charts showing the protein levels based on 2-DE and Western blot results in the bottom of panel

Fig. 3 — a The 2-DE gel showing the different spot intensities between OS-RC-2 and OS-RC-2-BM5. Among these altered proteins, 25 protein spots (P < 0.05) were noticeably down-regulated in the OS-RC-2-BM5 group (middle panel) and 75 protein spots (P < 0.05) were significantly up-regulated in the OS-RC-2-BM5 group on the right panel. b Results of quantitative Western blotting experiments performed for 26 proteins (change fold <0.5 and >1.9). The magnified images of protein spots from the 2-DE gels were shown on the upper part of each panel and the Western blot replicate results list below. The line charts showing the protein levels based on 2-DE and Western blot results in the bottom of panel