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. 2018 Feb 1;24(3-4):287–300. doi: 10.1089/ten.tea.2016.0535

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© Hiroko Iseoka et al. 2018; Published by Mary Ann Liebert, Inc.

This article is available under the Creative Commons License CC-BY-NC (http://creativecommons.org/licenses/by-nc/4.0). This license permits non-commercial use, distribution and reproduction in any medium, provided the original work is properly cited. Permission only needs to be obtained for commercial use and can be done via RightsLink.

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FIG. 1. — Flow cytometry of cardiomyogenically differentiated human iPSCs. (A) Cardiomyogenically differentiated human iPSCs were analyzed by flow-cytometry for cTnT and the cardiac-specific cell-surface marker CD172a. (B) Analysis of endothelial CD31, CD144, fibroblast TE-7, vimentin, αSMA, caldesmon, calponin, Nkx2.5, α-actinin, and cMHC expression in the cTnT-negative cell population. αSMA, α-smooth muscle actin; cMHC, cardiac myosin heavy chain; cTnT, cardiac troponin T; iPSCs, induced pluripotent stem cells. Color images available online at www.liebertpub.com/tea