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Expression of GFP-RNAi in the WT and rdr6-11 backgrounds. (A) Quantitative real-time PCR and (B) semi-quantitative RT-PCR were performed using a primer pair for an intron of the GFP-RNAi construct in the selected homozygous lines of the WT and rdr6-11 backgrounds. TUBULIN was used as an internal control for quantitative and semi-quantitative RT-PCR.
