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. 1999 Nov;67(11):5768–5774. doi: 10.1128/iai.67.11.5768-5774.1999

FIG. 3.

FIG. 3

The gel shown in the right panel of Fig. 1 was blotted and hybridized with a radiolabelled internal RvD2 PCR product (Table 1) generated from M. bovis BCG Pasteur genomic DNA. The probe bound only to the 7.9-kb M. tuberculosis H37Ra DraI fragment and not to M. tuberculosis H37Rv DNA, indicating that the 7.9-kb DraI fragment in M. tuberculosis H37Ra is due to the presence of RvD2. MW, molecular size markers.