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. 2016 Feb 27;15:124. doi: 10.1186/s12936-016-1177-x

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© Kumar et al. 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. 3 — Demonstration of successful PCR amplification of Plasmodium DNA using universal primers to detect an infection. Lane 1 & 3 (Negative controls); Lane 5 negative control (Nuclease free water); Lane 2 positive (1100 bp; Sample ID, SP328); Lane 4 (500 bp DNA ladder)