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. Author manuscript; available in PMC: 2009 Nov 29.
Published in final edited form as: Cancer Lett. 2007 Oct 30;259(1):28–38. doi: 10.1016/j.canlet.2007.09.018

Figure 1.

 Figure 1

Expression analysis of differential gene expression by real-time RT-PCR. Total RNA was reverse-transcribed and subsequently amplified by a real-time PCR using gene-specific primers. A fold-change in expression was calculated relative to LNCaP-C33 cells using GAPDH as an internal control by ΔΔCT method. Each experiment was repeated at least three times and data presented as mean ± standard deviation.