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. 2018 Apr 13;8:5969. doi: 10.1038/s41598-018-24320-3

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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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Saturation binding of apoE isoforms to the ELISA polystyrene surface. Variable concentrations (0–800 nM) of the three different recombinant apoE isoforms were added to ELISA plate wells, and incubated for 2 h at RT. After blocking, bound apoE was detected with a polyclonal pan-apoE antibody, followed by horseradish peroxidase-labelled anti-rabbit IgG. Error bars represent the standard deviation of duplicated measures. The graph shows a representative experiment of four independent tests performed by duplicate. The inset shows the same data represented from apoE concentrations in the 0–128 nM range.