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. 2019 Jul 8;12(7):984–993. doi: 10.14202/vetworld.2019.984-993

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Copyright: © Sobur, et al.

Open Access. This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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.

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Figure-1 — Polymerase chain reaction (PCR) amplification of 16S rRNA of Escherichia coli and invA gene of Salmonella spp. (a) PCR amplification of 16S rRNA of E. coli. Lane M: 100 bp DNA Marker, 1: Negative control, 2: Positive control, and 3-7: Representative E. coli isolates. (b) PCR amplification of invA gene of Salmonella spp. Lane M: 100 bp DNA Marker, 1: Negative control, 2-6: Representative Salmonella spp. isolates, and 7: Positive control.