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. 2020 Nov 20;10:20283. doi: 10.1038/s41598-020-77497-x

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© The Author(s) 2020

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 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/.

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Binding of DC-SIGN-Fc chimera protein to immobilized ES L1 products. (A) Dose dependent manner of DC-SIGN-Fc binding to microwell plate coated with ES L1. (B) The specificity of DC-SIGN-Fc binding to ES L1 demonstrated by the inhibition of the reaction with EDTA and mannan. The results are presented as mean values of two independent experiments. Differences were analysed for significance by one-way ANOVA with the Bonferroni’s multiple comparison test: ***p < 0.001. (C) DC-SIGN-Fc recognizes 49, 53 and 66 kDa ES L1 glycoproteins in Western blot.