The Plant Pathology Journal

Fig. 1.

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Fig. 1. Amplification of the expected PCR products (A) Products from bacterial genomic DNA. (B) Products from suspensions of five strains of Burkholderia glumae (Lane 1–5) amplified using Bglu3-f and Bglu3-r primers and six strains of Burkholderia gladioli (Lane 6–11) amplified using Bgla9-f and Bgla9-r primers. Lane 12 is a negative control. Specific bands were clearly visible on the 2% agarose gel at 174 bp for B. glumae and 289 bp for B. gladioli. M denotes the 1 kb DNA ladder.
The Plant Pathology Journal 2018;34:490-8
© 2018 The Plant Pathology Journal