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. 2017 Oct 11;8:1275. doi: 10.3389/fimmu.2017.01275

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Copyright © 2017 Gimenez, Lima, Françoso, Denapoli, Panatieri, Bargieri, Thiberge, Andolina, Nosten, Renia, Nussenzweig, Nussenzweig, Amino, Rodrigues and Soares.

This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

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Recognition of native protein in Plasmodium vivax isolates. Indirect immunofluorescence analysis was performed using pool of sera (diluted 1:100) from C57BL/6 mice immunized with (A) yPvCSP-All epitopes, (B) protein mixture or (C) phosphate-buffered saline (PBS) in adjuvant, as a negative control. (D) As a control positive anti-PvCSP-VK210 (MAb 2F2) was used. Microscope slides containing wild-type P. vivax were obtained from Thailand isolates. Antibody binding was detected with secondary Alexa 568-labeled antibody (red) and nuclei were visualized by DAPI staining.