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. 2018 Mar 19;15(5):7537–7544. doi: 10.3892/ol.2018.8293

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Copyright: © Zhang 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. — Analysis of Bcl-2 and Bcl-xL protein expression in GEC-BARF1 cells. Western blotting of (A-a) Bcl-2 and (A-b) Bcl-xL expression, and quantitative analysis of (A-c) Bcl-2 and (A-d) Bcl-xL expression in GEC-BARF1 cells compared with GEC-SG cells. (B-a, B-b, C-a, C-b, D-a and D-b) Western blotting and quantitative analysis of (B-c, C-c and D-c) Bcl-2 and (B-d, C-d and D-d) Bcl-xL protein expression levels in SGC-BARF1 treated with SP600125, SB203580 and U0126 compared with DMSO, respectively. Data were expressed as the mean ± standard deviation from three independent experiments. *P<0.05, **P<0.01 vs. GEC-SG. ^#P<0.05, ^##P<0.01 vs. DMSO control. DMSO, dimethyl sulfoxide; Bcl, B-cell lymphoma.