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. 2018 Aug 1;8:11568. doi: 10.1038/s41598-018-29969-4

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© The Author(s) 2018

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

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Measurement of protein expression of candidate detection markers by western blot on days 0, 2, 4, 6, 8 (9) post-blood meal in mosquitoes. Two oocysts were loaded per lane and Pf. conserved Plasmodium protein (A), Pf. receptor for activated C kinase homolog (RACK) (B), Pf. thioredoxin peroxidase 1 (TRP1) (C), Pf. von Willebrand factor A-domain-related protein (WARP) (D), Pf. circumsporozoite protein (E) and negative antibody control (F) were detected using monoclonal antibodies specific for the respective Pf recombinant proteins. Details of the secondary antibodies and Western blot reagents are provided in the Methods section. Expression levels were quantitated by measuring the intensities of protein bands in individual lanes using MetaMorph Software (version 6.1) and are represented as IOD units.