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. 2010 Jun 10;6(6):e1000951. doi: 10.1371/journal.ppat.1000951

Figure 9. Expression of p16INK4A is increased in CtBPM LCLs relative to revertant and WT LCLs.

Figure 9

(A) E3CtBP, 3ACtBP, 3CCtBP and two revCtBP LCLs were harvested 28 days after the infection of primary B cells with the recombinant EBVs. RNA was extracted and the relative levels of CDKN2A transcripts were quantified by qRT-PCR. (B) RNA was extracted from two established E3CtBP LCLs, two 3ACtBP LCLs, 3CCtBP LCL, a revertant (revCtBP) and a WT-EBV LCL. The relative levels of p16INK4A transcripts were quantified by qRT-PCR. (C) Western blot analysis of protein extracts from two E3CtBP LCLs, two 3ACtBP LCLs and a 3CCtBP LCL all established from a single donor. A revertant (revCtBP) and a WT-EBV LCL are shown for comparison. Levels of p16INK4A (p16) are shown relative to γ-tubulin (γ-tub).