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. 2017 Oct 2;14:189. doi: 10.1186/s12985-017-0856-8

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© The Author(s). 2017

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 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.

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Fig. 1 — Preliminary determination of serotype specificity of selected anti-E mAbs by indirect ELISA. Four serotypes of DV (DV1, Hawaii; DV2, NGC; DV3, H87; DV4, H241) and JEV (T1P1)-infected C6/36 cell lysates, either native (dark column) or heat-treated (grey column, 95 °C for 10 min) DV1 E395 protein were coated on ELISA plates and reacted with (a) DV1-E1 and (b) DV1-E2 mAbs, respectively. Error bars indicate standard deviations (SD)