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. 2016 Sep 13;12(1):202. doi: 10.1186/s12917-016-0809-2

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© The Author(s). 2016

Open AccessThis 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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Fig. 7 — Specificity of the LAMP outer primers (F3 and B3) for amplification of the Sudanese strains of EG-complex using conventional PCR. Visualization of the 200-bp specific DNA PCR products on ethidium bromide-stained agarose gels. Lane MW: molecular weight marker; lanes 1–2: 1.0 pg E.ortleppi (G5) DNA (positive control); Lane 3–4: 1.0 pg E.canadensis (G6) DNA; Lane 5: nucleic acid-free water