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. 2020 Feb 21;13:93. doi: 10.1186/s13071-020-3965-y

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© The Author(s) 2020

Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. 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 in a credit line to the data.

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Fig. 1 — Eimeria acervulina sporozoite protein 2-dimensional gel electrophoresis (2-DE) profile demonstrated by silver staining. The soluble sporozoite proteins (200 μg) of E. acervulina were first resolved by isoelectric focusing (IEF) using a 24 cm immobilized pH gradient (IPG) strip (pH 3–10). Then, sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE) (12.5%) was used to separate the proteins by size followed by silver staining. The Y-axis shows the protein Mr. range between 11 and 180 kDa and X-axis indicates the protein pI range between 3 and 10. Data represent results from 2 independent experiments