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. Author manuscript; available in PMC: 2009 Oct 14.
Published in final edited form as: Oncogene. 2001 Aug 2;20(34):4629–4639. doi: 10.1038/sj.onc.1204680

Figure 6.

Figure 6

Lack of DNA strand breaks in Dex-treated C7-MycER™ cells, (a–d) CEM-C7-14 (a, b) or C7-MycER™ #22 (c, d) cells were treated with ethanol (a, c) or 100 nM Dex (b, d) for 72 h. Samples were harvested, and analysed for nicked DNA by TUNEL assay. Flow cytometry was carried out using a FACScan and Cell Quest 1.2 software from Becton Dickinson as described in Materials and methods, (e) Time course of DNA nicking. CEM-C7-14. C7-MycER™ mass culture and C7-MycER™ #22 cells were treated for 72 h with 100 nM Dex, and aliquots were harvested every 12–24 h for TUNEL analysis as described above