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A) Predicted secondary structure surrounding the BDF2 editing site. B) Sequence traces for RT-PCR products of edited region in 232 nt BDF2-derived RNA incubated with 75 nM ADAR1-D for 0 or 60 minutes. C) Plot of kobs as a function of ADAR1-D concentration for reactions containing 10 nM 232 nt BDF2-derived RNA.
