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. 2000 Jan;182(2):432–438. doi: 10.1128/jb.182.2.432-438.2000

FIG. 3.

FIG. 3

DNase I footprinting assays. All DNA fragments were 3′ end labeled with [α-32P]dCTP on one strand and were incubated in the presence of Co2+ (300 μM) and DtxR (1000 nM for pIRP3 and its variants; 200 nM for pIRP1 and its variant). (A) Lanes: 1, pIRP1 with no DtxR; 2, pIRP1 with DtxR; 3, pIRP1 T(+7)C with DtxR. (B) Lanes: 1, pIRP3 with no DtxR; 2, pIRP3 with DtxR; 3, pIRP3 C(+7)T with DtxR; 4, pIRP3 C(+7)T/A(−7)G with DtxR. Brackets indicate sequences protected by DtxR from DNase I digestion.