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. 2018 Feb 13;17(4):5860–5868. doi: 10.3892/mmr.2018.8606

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Copyright: © Peng 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 1. — Purity analysis of the isolated cells. Settings of the (A) T cell and (B) CD4 flow cytometer gates. (C) Ratio of CD4⁺CD25⁺ cells in CD4⁺ T cells. Sample: T cells. (D) Ratio of CD4⁺CD25⁺ cells in CD4⁺ T cells. Sample: CD4⁺CD127⁻ cells. (E) Ratio of CD4⁺CD25⁺ cells in CD4⁺ T cells. Sample: CD25⁻ cells. (F) Ratio of CD4⁺CD25⁺ cells in CD4⁺ T cells Sample: CD4⁺CD25⁺ cells. FSC, forward scatter; CD, cluster of differentiation; FITC, fluorescein isothiocyanate; UR, upper right; UL, upper left; LL, lower left; LR, lower right; APC, allophycocyanin; SSC, side scatter.