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. 2000 May;38(5):2001–2004. doi: 10.1128/jcm.38.5.2001-2004.2000

FIG. 5.

FIG. 5

Agarose gel electrophoresis of multiplex PCRs with DNAs containing several virulence genes (+) and DNAs without the genes (−). The genes and PCR primers in each lane, from left to right, were VT1, VT2, VT2e, and eaeA in the 1st lane; VT1, VT2, VT2e, eaeA, CNF2, and Einv in the 2nd and 3rd lanes; VT1, VT2, VT2e, eaeA, CNF1, and Eagg in the 4th and 5th lanes; VT1, VT2, VT2e, eaeA, LTI, and STI in the 6th and 7th lanes; VT1, VT2, VT2e, eaeA, CNF2, Einv, LTI, and STI in the 8th and 9th lanes; and VT1, VT2, VT2e, eaeA, CNF1, Eagg, LTI, and STI in the 10th and 11th lanes. Lane S, DNA standards.