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. 2017 Dec 7;7:17174. doi: 10.1038/s41598-017-17488-7

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© The Author(s) 2017

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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Conoidin A inhibits PRDX activity in mouse spermatozoa. (A) Density of PRDXs-SO₃ in control and conoidin A-treated samples with exposure to glucose oxidase. (B) Density of PRDXs-SO₃ in control and conoidin A-treated samples without exposure to glucose oxidase. (C) Representative western blot of PRDXs-SO₃ probed with anti-peroxiredoxin-SO₃ antibody (uncropped blots are presented in Supplementary Fig. 1). (D) Representative western blot of PRDXs-SO₃ probed with anti-peroxiredoxin-SO₃ antibody (uncropped blots are presented in Supplementary Fig. 1). Data represent mean ± SEM, n = 3. Values with superscripts (^a,b) are significantly different between control and conoidin A-treatment groups by one-way ANOVA (P < 0.05) with Tukey’s multiple comparison test.