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. 2019 Jun 27;10:193. doi: 10.1186/s13287-019-1303-0

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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. 4 — PC-iPS contributes to mouse late blastocyst TE and ICM in vitro. a Injection GFP labeled PC-iPS cells to 4- to 8-cell embryos, scale bar 200 μm, 20 μm. b GFP-labeled PC-iPS cells contribute to the TE and ICM, scale bar 20 μm. c Immunocytochemistry analysis of CDX2 and NANOG in chimeric mouse late blastocyst, scale bar 20 μm