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. 2017 Oct 19;8(61):103449–103464. doi: 10.18632/oncotarget.21968

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Copyright: © 2017 Zheng et al.

This is an open-access article distributed under the terms of the Creative Commons Attribution License 3.0 (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

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Endogenous ING5 expression was screened in several kinds of ovarian cancer cells, including SKOV3, SKOV3/DDP, OVCAR3, OVCA3, HO8910, HO8910-pm, and ES-2, evidenced by RT-PCR (A), Western blot (A, B), immunofluorescence and nucleocytosolic fraction (C). After transfection of pEGFP-N1-ING5, ING5 expression became strong in HO8910, HO8910-PM, A2780 and A2780/T cells by immunofluorescence (D), RT-PCR (E), and Western blot (F). ^*p < 0.05, compared with transfectants.

Endogenous ING5 expression was screened in several kinds of ovarian cancer cells, including SKOV3, SKOV3/DDP, OVCAR3, OVCA3, HO8910, HO8910-pm, and ES-2, evidenced by RT-PCR (A), Western blot (A, B), immunofluorescence and nucleocytosolic fraction (C). After transfection of pEGFP-N1-ING5, ING5 expression became strong in HO8910, HO8910-PM, A2780 and A2780/T cells by immunofluorescence (D), RT-PCR (E), and Western blot (F). ^*p < 0.05, compared with transfectants.