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. 2015 Jan 23;53(2):653–656. doi: 10.1128/JCM.01963-14

FIG 2.

FIG 2

Four clinical isolates analyzed by mPCR for Aeromonas species identifications. Each primer set was designed to be specific for the particular species and to have a unique amplicon size when analyzed by agarose gel electrophoresis. Also included in the mPCR was a primer set targeting 16S rRNA genes, which served as an internal PCR control (461 bp). Lane 1, 50-bp DNA marker; lane 2, A. caviae (70 bp); lane 3, A. media (99 bp); lane 4, A. hydrophila (144 bp); and lane 5, A. veronii (244 bp).