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. 2015 Dec 3;11(2):933–938. doi: 10.3892/ol.2015.3996

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Copyright: © Wang 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. — FOXC1 expression in serous ovarian carcinoma cell lines. (A) FOXC1 mRNA levels in SKOV-3 and HO-8910 cell lines. (B) FOXC1 protein levels in SKOV-3 and HO-8910 cell lines. Ns and Nh represent nuclear protein of SKOV-3 and HO-8910 cells, respectively; Cs and Ch represent cytoplasmic protein of SKOV-3 and HO-8910 cells, respectively. β-actin was used as an internal control in western blot analysis. (C) Left panel: Nuclear and cytoplasmic immunostaining of FOXC1 was observed in SKOV-3 cells, although staining was less intense in the cytoplasm than in the nucleus, which was in accordance with the results of western blot analysis. Right panel: Nuclear and cytoplasmic staining of FOXC1 was observed in HO-8910 cells, although staining was less intense in the cytoplasm than in the nucleus, which was in accordance with the results of western blot analysis.