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Confirmation of bcr1 and bcr3 of clinical samples after RT-LAMP assay. The RT-LAMP products of clinical sample RNAs of S-1 (A) and S-5 (B) were incubated with (+) or without (−) DdeI at 37 °C for 120 min, followed by deactivation at 70 °C for 15 min and separation by 1.5% agarose gel electrophoresis (100 V, 35 min). M, 100-bp ladder size marker; RT-LAMP, reverse transcription loop-mediated isothermal amplification.
