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. 2015 Mar 7;14:106. doi: 10.1186/s12936-015-0619-1

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© Arévalo-Pinzón et al.; licensee BioMed Central. 2015

This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. 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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r Pv RON5 expression and antigenicity studies. (A) rPvRON5 expression and purification. Lane 1, rPvRON5 purified by affinity chromatography with Coomassie blue staining. A single ~33 kDa band was observed which coincided with the expected molecular weight. Lane 2, WB recognition of rPvRON5 using anti-polyhistidine monoclonal antibody. (B) P. vivax patients’ sera reactivity with rPvRON5. Top panel, recognition of recombinant protein by WB. H: reactivity by monoclonal anti-polyhistidine serum. Lanes 1 to 11, recognition of rPvRON5 by sera from P. vivax-infected patients. A single ~33 kDa band can be seen. Lanes 12 to 15, sera from healthy individuals. R: Polyclonal serum 2 reactivity with rPvRON5. Bottom panel, ELISA recognition of rPvRON5 by sera from P. vivax-infected patients (grey bars) and healthy individuals (black bars).