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. 2019 Mar 18;17(5):3989–3998. doi: 10.3892/etm.2019.7405

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Copyright: © Du 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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Figure 3. — Flow cytometric analysis and proliferation assay. (A) Flow cytometric analysis plots of c-kit⁺, CD34⁺ and sca-1⁺ cells isolated from MI and sham mice. (B-D) Expression analysis of c-kit⁺, CD34⁺ and sca-1⁺ in BM cells. ***P<0.001 as indicated (n=6 for each group). (E) CellTiter 96^® AQueous One Solution reagent was used to assess c-kit⁺ BM cells seeded on P(LLA-CL) or SF/P(LLA-CL) or those cultured without scaffolds at indicated time points. *P<0.05 (n=6 for each group). SF, silk fibroin; P(LLA-CL), poly(L-lactic acid-co-ε-caprolactone); MI, myocardial infarction; BM, bone marrow; CD, cluster of differentiation; CD117, c-kit; sca-1, stem cell antigen-1; OD, optical density.