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Fig. 4 | Journal of Genetic Engineering and Biotechnology

Fig. 4

From: Loop-mediated isothermal amplification: a rapid molecular technique for early diagnosis of Pseudomonas syringae pv. syringae of stone fruits

Fig. 4

The comparison of electrophoresis-based methods of PCR and LAMP products in terms of sensitivity. Lane 1, PCR product without dilution 10 (200 ng/μl); lane 2, PCR product diluted by 10− 1 (20 ng/μl); lane 3, PCR product diluted by 10− 3 (2 ng/μl); lane 4, PCR product diluted by 10− 3 (0.2 ng/μl); lane 5, PCR product diluted by 10− 4 (0.02 ng/μl); and lane 6, 1 kb DNA ladder. Lane 7, LAMP product without dilution 10 (1 ng/μl); lane 8, LAMP product diluted by 10− 1 (0.1 ng/μl); lane 9, LAMP product diluted by 10− 2 (0.01 ng/μl); lane 10, LAMP product diluted by 10− 3 (0.001 ng/μl); lane 11, LAMP product diluted by 10− 4 (0.0001 ng/μl); and lane 12, LAMP product diluted by 10− 5 (0.00001 ng/μl)

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