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. 2018 Apr 3;42(1):131–140. doi: 10.3892/ijmm.2018.3610

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Copyright: © Ke et al.

This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.

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Effects of LIF on the apoptosis of marmoset iPSCs in culture. (A) Cell apoptosis was analyzed using flow cytometric analysis of FITC Annexin V staining. FITC Annexin V and PI-positive cells were analyzed by flow cytometry. (B) The majority of marmoset iPSCs were FITC Annexin V and PI negative. Apoptosis in the treatment group was 4.81±1.51% and in the control group was 4.25±1.01%. No significant difference in apoptosis was found. Q1, necrotic cells; Q2, late apoptosis; Q3, early apoptosis; Q4, viable cells; LIF, leukemia inhibitory factor; iPSCs, induced pluripotent stem cells; bFGF, basic fibroblast growth factor.