Fig. 4From: 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 principle of LFD. The illustration shows the LAMP product is immobilised on the membrane by streptavidin, followed with signal generation by conjugated GNPs that bind on fluoresceinBack to article page