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. 2011 Mar 16;286(19):16984–16991. doi: 10.1074/jbc.M111.228833

FIGURE 3.

FIGURE 3.

Equilibrium substrate binding by RNase H2 WT. The FAM-labeled duplexes (1 nm) were incubated with increased concentrations of RNase H2 WT and the observed relative fluorescence anisotropy Aobs = AAo/Amax was determined as described under “Experimental Procedures” for the 1-ribo (○, long dashes), 4-ribo (▴, short dashes), 20-ribo (△, dots), and DNA (●, solid line). The fluorescence anisotropy data were fit to a single hyperbola to derive KD values (inset).