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. 2023 Jan 28;24(3):2511. doi: 10.3390/ijms24032511

Figure 5.

Figure 5

Reverse transcription-recombinase polymerase amplification (RT-RPA) optimization for potato leafroll virus (PLRV) detection using forward and reverse primer LRRPAF3/R3-Set C. The RT-RPA amplified products on (a) a PCR machine and (b) a water bath using a cDNA template at a temperature of 40 °C and a duration range of 10, 20, 30, 40 and 50 min. Likewise, the RT-RPA amplified amplicons using total RNA (1 μL) in (c) a PCR machine and (d) a water bath under the same conditions of temperature and duration. Optimization of magnesium acetate concentrations ranging from 12 mM to 20 mM under a similar setup of (e) thermal cycler and (f) water bath. Lane M: 50 bp ladder; HC: healthy control.