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. 2017 Feb 28;8:247. doi: 10.3389/fpls.2017.00247

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Copyright © 2017 Mardanova, Blokhina, Tsybalova, Peyret, Lomonossoff and Ravin.

This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

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Expression and purification of M2eHBc using the pEff vector. Coomassie brilliant blue stained gel (A) and Western blot (B) of proteins isolated from N. benthamiana leaves and separated by SDS-PAGE. M, molecular weight marker (kD); (1) total soluble proteins isolated from leaves infiltrated with vector pEff-M2eHBc; (2) total soluble proteins isolated from uninfiltrated leaves. Antibodies against M2e were used in Western blotting. (C) Transmission electron microscopy of plant-produced M2eHBc virus-like particles. The grid was negatively stained with 2% (w/v) uranyl acetate and the scale bar is shown.