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. 2005 Mar;73(3):1561–1567. doi: 10.1128/IAI.73.3.1561-1567.2005

FIG. 3.

FIG. 3.

Detection of the adaA gene from various isolates of C. burnetii by PCR with primers P28F-P28R. Shown is an ethidium bromide-stained agarose gel electrophoretogram of PCR-amplified products. Lane 1, molecular size markers (100-bp DNA ladder); lanes 2 to 9, isolates originating from ticks, milk, and humans with acute Q fever (Nine Mile, Ohio, California, El Tayeb, Africa, Panama, Turkey, and Giround, respectively); lanes 10 to 14, isolates originating from a goat and humans with chronic Q fever (Priscilla, KQ154, KoQ229, SQ217, and GQ212, respectively); lane 15, Dugway isolate.