Figure 2. RNase activity assay.
The RNase activity of purified hrRNASET2 was assayed by observing the change in fluorescence intensity of toluidine blue on binding with yeast RNA. hrRNASET2 samples (10 μl) were placed over a plate containing 10 ml 0.1% yeast RNA and 0.8% agarose, and incubated for 30 min (37°C). Agarose plates were stained with 0.02% (w/v) toluidine blue to detect RNase activity. RNase activity was quantified by placing samples (50 μl) in 50 μl 100 mM sodium acetate buffer (pH 4.5) that contained 4 mg/ml yeast RNA.