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. 2019 Jul 17;10:211. doi: 10.1186/s13287-019-1316-8

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© The Author(s). 2019

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 — Relative expression of pluripotency genes in established iPSC lines. Relative arbitrary expression values are normalized to the negative control sample and indicated as fold change. Endogenous OCT4 and SOX2 expressions were analyzed differentially to demarcate any expression originating from the transgenes. The cumulative expressions were given for all the other genes. The expressions of pluripotency genes were detectable in all of the tested lines for all time-points, with no significant variations between the lines (n = 47 iPSC lines, three lines from each sample at different time points; P5-P20)