Figure 2 | Scientific Reports

Figure 2

From: Rapid isothermal duplex real-time recombinase polymerase amplification (RPA) assay for the diagnosis of equine piroplasmosis

Figure 2

Real-time fluorescence curves of RPA assay using different primers and probes. (a) B. caballi-bc48-F1/R2 (line 1) and Primer B. caballi-bc48-F2/R1 (line 2), targeting the B. caballi bc48 gene for pUC57-bc48 plasmid DNA; (b) Primer T. equi-ema-F1/R1 (line 1) and T. equi-ema-F2/R2 (line 2), targeting T. equi ema-1 gene for pUC57-ema plasmid DNA. (c) Primer B. caballi-Bc18S-F1/R1 assay for pUC57-Bc18S plasmid DNA (line a), pUC57-Te18S plasmid DNA (line b) and T. equi-Bc18S-F1/R1 assay for pUC57-Bc18S plasmid DNA (line c); (d) Primer B. caballi-Bc18S-F2/R2 for pUC57-Bc18S plasmid DNA (line 1), pUC57-Te18S plasmid DNA (line 1-Te), B. caballi-Bc18S-F2/R3 (line 2-Te), B. caballi-Bc18S-F3/R2 (line 3-Te) and B. caballi-Bc18S-F3/R3 (line 4-Te) for pUC57-Te18S plasmid DNA; (e) Primer T. equi-18S-F2/R2 for pUC57-Te18S plasmid DNA (line 1-Te), pUC57-Bc18S plasmid DNA (line 1-Bc), T. equi-18S-F3/R2 for pUC57-Te18S plasmid DNA (line 2-Te), and pUC57-Bc18S plasmid DNA (line 2-Bc).

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