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. 2015 Dec 1;6:235. doi: 10.1186/s13287-015-0235-6

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© Rakian et al. 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. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

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Fig. 2 — Cell number of primary BM-MSCs after culture in SFM or SCM for 14 days. Primary cultures of BM-MSCs were grown for 14 days on TCP, BM-ECM, or CELLstart™ in SCM or SFM. At harvest, cell number was determined by cell counting after staining with trypan blue. SCM was superior to SFM in promoting cell proliferation, but the overall trend observed with the three culture surfaces remained similar. *P < 0.05, significantly different from BM-ECM and CELLstart™; ^† P < 0.05, significantly different from BM-ECM. BM-ECM bone marrow-derived extracellular matrix, BM-MSC bone marrow-derived mesenchymal stem cell, SCM serum-containing media, SFM serum-free media, TCP tissue culture plastic