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. 2018 Jun 1;34(3):191–198. doi: 10.5423/PPJ.FT.03.2018.0055

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© The Korean Society of Plant Pathology

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted noncommercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

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Fig. 1 — DNA amplification curves of representative strains of Erwinia amylovora (Ea), E. pyrifoliae (Ep), and Pseudomonas syringae pv. syringae (Pss) by DS-LAMP (A) and Bühlmann-LAMP (B) carried out with Genie III (OptiGene Ltd, West Sussex, UK). Purified genomic DNA (10 ng) was used; Ea YKB 12316 (black circle), Ea YKB 12317 (hollow Circle), Ep KACC 13952 (black square), Ep YKB 12325 (hollow square), Pss SHPS 022 (black triangle), Pss WSPS 039 (hollow triangle). Distilled water was as a negative control (black line).