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. 2018 Jun 25;14:201. doi: 10.1186/s12917-018-1537-6

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© The Author(s). 2018

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 — Characterization of the MAb 9E4 against TMUV. a Indirect immunofluorescence assay and immunocytochemistry of MAb 9E4 against duck TMUV, Japanese encephalitis virus and batai virus-infected BHK-21 cells. b Western blot analysis of MAb 9E4 reactivity against the virus particle. 1&2: Virus particle under non-reducing conditions or reducing conditions; 3&4: BHK-21 cell lysates under non-reducing conditions or reducing conditions; c Western blot analysis of MAb 9E4 reactivity against disulfide bonds reformed recombinant expression protein under non-reducing condition. 1: pET 32α tag protein; 2: E ectodomain; 3: E domain I/II; 4: E domain III