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. 2006 Sep 29;34(19):5395–5401. doi: 10.1093/nar/gkl649

Figure 2.

Figure 2

In vivo DNase I sensitivity determined by Southern hybridization analysis. DNA harvested from mycelium taken from each time point was treated with increasing amounts of DNase I, digested to completion with restriction enzymes and used in Southern hybridization assays. Blots were hybridized with mixtures of probes for (A) rbnH, redD, rlpA and sti1 and (B) actII-orf4, afsQ2, hrdB and rpmG3. The positions of the genomic bands for each gene are indicated, with the amount of DNase I used increasing from left to right.