Development and comparison of loop-mediated isothermal amplification with quantitative PCR for the specific detection of Saprolegnia spp.
Fig 8
Direct detection of zoospores.
A. qPCR and B. LAMP. One and ten zoospores were used in each reaction, S. salmonis DNA (10 ng/μl) was used as the positive control while no template control (NTC) was used as the negative control. Each sample was performed in triplicate and was repeated three times.