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. 2017 Sep 1;8:69. doi: 10.1186/s40104-017-0201-5

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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 — a SDS-PAGE analysis showing expression of recombinant OVGP1. Lane 1: Uninduced, lane 2: Molecular weight marker, lane 3: Induced, lane 4: Pellet, lane 5: Soluble fraction; (b) SDS-PAGE analysis of His-tag affinity purified recombinant OVGP1 (indicated by arrow). Lane 1: Molecular weight marker, lane 2–5: Eluted fractions for partially purified His- tagged recombinant OVGP1; (c) Anion- exchange purification of recombinant OVGP1 (indicated by arrow). Lane 1: Unbound fraction, lane 2: Molecular weight marker, lane 3–9: Eluted fractions for partially purified His- tagged recombinant OVGP1; and (d) Gel filtration purification representing single band (indicated by arrow) for purified His- tagged recombinant OVGP1, lane 1: Unstained molecular weight marker, lane 2: purified His- tagged recombinant OVGP1; (e) Western blot analysis of purified His-tagged recombinant OVGP1. Lane 1: Prestained molecular weight marker, lane 2: purified His- tagged recombinant OVGP1