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. Author manuscript; available in PMC: 2011 May 28.
Published in final edited form as: J Mol Biol. 2010 Apr 7;399(1):182–195. doi: 10.1016/j.jmb.2010.03.054

Figure 2.

Figure 2

Preferential orientation for DNA cleavage by FPV resolvase on Junction 1S. DNA oligonucleotides were 5'-end labeled with 32P on the strands indicated above the gels. Resolvase enzymes studied are marked above the gel lanes. Fowlpox resolvase, Cce I protein or T7 endonuclease I (New England Biolabs, Beverley, MA) were added to a solution containing HJ1S DNA (final concentrations; 10 nM resolvase, 10 nM Cce I, 2U of T7 endonuclease and 2nM HJ1S DNA substrate). Reaction mixtures were incubated at 37 °C for 30 min. Products of the reactions were separated on urea-containing 10% polyacrylamide gels by electrophoresis in 1X TBE buffer and visualized by autoradiography.