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. 2013 Jul 31;8(7):e68399. doi: 10.1371/journal.pone.0068399

Figure 3. qRT-PCR using protocols shown in figure 2D and E can detect changes in splicing induced by splicing factor knockdown.

Figure 3

A. Ctmax-Ct for cDNA extracted from prostate cancer (PC3) cells with lentiviral knockdown of SRPK1 or scrambled. B. Amount of VEGF calculated from standard curves in Figure 2. C. Amount of VEGF-A165b identified by Exon 8b primers (VEGF-A165b) or that calculated from mispriming of VEGF-A165a. D. Proportion of VEGF that is VEGF-A165a or VEGF-A165b in control and knockdown cells. Values are Mean±SEM (n = 2). 3E. qPCR for VEGF-A165a on commercially available cDNAs from 2 different companies (open bars) or cDNA reverse transcribed from freshly extracted human kidney RNA (solid bar). 3F qPCR for VEGF-A165b on commercially available cDNAs from 2 different companies (open bars) or cDNA reverse transcribed from freshly extracted human kidney RNA (solid bar).