Fig. 3From: Loop-mediated isothermal amplification (LAMP) reaction as viable PCR substitute for diagnostic applications: a comparative analysis study of LAMP, conventional PCR, nested PCR (nPCR) and real-time PCR (qPCR) based on Entamoeba histolytica DNA derived from faecal sampleSchematic illustration of the formation of double-labelled amplicon (LAMP product) works as the analyte for LFD detectionBack to article page