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. 2016 Mar 21;9:166. doi: 10.1186/s13071-016-1457-x

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© Lu 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. 1 — Electrophoresis of PCR amplicons obtained from different genomic DNA sources using the Nd5-2 primers. Lane 1: S. haematobium; Lane 2: S. japonicum; Lane 3: S. rodhaini; Lane 4: uninfected B. pfeifferi; Lane 5: S. mansoni-infected B. pfeifferi; Lane 6: uninfected B. sudanica; Lane 7: S. mansoni-infected B. sudanica; Lane 8: Negative control; Lane 9: Positive control (S. mansoni genomic DNA); Lane M: GeneRuler 100 bp DNA ladder (Thermo Scientific, USA). Values on the right are in base pairs