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. 2008 Nov 14;283(46):31649–31656. doi: 10.1074/jbc.M806155200

FIGURE 8.

FIGURE 8.

The TREX1R114H/R114H and TREX1WT/R114H enzymes do not inhibit the TREX1MWT dsDNA degradation activity. Exonuclease reactions (20 μl) were prepared containing nicked dsDNA plasmid 1 (10 μg/ml = 1.6 nm nicks) and no enzyme (lane 2), the indicated concentration of TREX1WT only (lane 3), or a mixture of TREX1WT with the indicated increased concentrations of TREX1R114H/R114H (lanes 4–8), and TREX1WT/R114H (lanes 9–13). The reactions were 30 min, and the products were subjected to electrophoresis on agarose gels. Lane 1 contains the supercoiled dsDNA plasmid 1. The positions of migration of Form I supercoiled dsDNA (dsDNA), Form II nicked dsDNA (Nicked dsDNA), and circular ssDNA (ssDNA) are indicated.