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. 2018 Aug 24;97(34):e11881. doi: 10.1097/MD.0000000000011881

Figure 2.

Figure 2

Agarose gel electrophoresis of polymerase chain reaction (PCR) products derived from the Coxiella burnetii IS1111a gene. Amplification of bacterial DNA using Q fever-IS1111a primers to detect C burnetii. Gel electrophoresis of end-point PCR products (202 bp). M: 50 bp DNA size marker; 1–20: DNA samples from patients with culture-negative infective endocarditis (IE); 21–40: DNA samples from patients with culture-positive IE and the negative controls (N).