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. 2020 Mar 4;16:76. doi: 10.1186/s12917-020-02297-4

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© The Author(s) 2020

Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

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Fig. 3 — Amplification specificity of the primer pairs. Agarose gel images showing the RPA amplification results for the different bacterial templates by the F1/R, F2/R and F6/R primer pairs. The species of bacteria are indicated on top of each lane. The NTC lane is the no-template control. The size of each band of the DNA ladder is indicated on the right of the gel image