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. 2016 May 31;8(6):119. doi: 10.3390/v8060119

Figure 4.

Figure 4

Comparison of transcription efficiency of the horse RNA PolI promoter in FEL, MDCK, and DF-1 cells. The transfection method and the amount of each plasmid was the same as in Figure 2B. The relative luciferase activities associated with the pLW500-NPluci construct in FEL cells (A), the pdoPolI-NPluci construct in MDCK cells (B) and the pchPolI-NPluci construct in DF-1 cells (C) were set as 100%. The relative luciferase activities associated with the pLW0-NPluci construct containing no RNA PolI promoter was used in FEL cells (A); MDCK cells (B); and DF-1 cells (C) as control, respectively. Each experiment was repeated three times.