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Fig. 3 | Parasites & Vectors

Fig. 3

From: Rapid detection of Galba truncatula in water sources on pasture-land using loop-mediated isothermal amplification for control of trematode infections

Fig. 3

Lower limit of detection for G. truncatula conventional PCR. This was determined by making 10-fold dilutions ranging from 104–106 of 50 ng/μl G. truncatula genomic DNA extract samples. Lane M: 100 bp DNA Ladder (Thermo Fisher Scientific); Lane +: positive control; Lane −: no-template negative control

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Parasites & Vectors

ISSN: 1756-3305

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