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. 2020 Feb 21;18:e00074. doi: 10.1016/j.fawpar.2020.e00074

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© 2020 The Authors

This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).

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Fig. 2 — Agarose gel electrophoresis of DNA fragments generated by multiplex PCR with the Sarcocystis spp. positive samples isolated from cattle striated muscle in the Department of Veterinary Science of Turin University. Lanes 1 to 5 correspond respectively to: the simultaneous presence of S. bovifelis, S. hominis, S. cruzi and S. hirsuta (lane 1); S. bovifelis (lane 2); S. cruzi (lane 3); S. hominis (lane 4); S. hirsuta (lane 5). In each sample, the Sarcocystis spp. fragment is generated. Lane “M” correspond to the 100 bp DNA molecular-weight size marker (Invitrogen, Thermo Fisher Scientific, Vilnius, Lithuania).