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. 2019 Dec 24;9(1):29. doi: 10.3390/plants9010029

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© 2019 by the authors.

Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).

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(a) SDS-PAGE gel and (b) Western blot of HEV 110–610 with anti-HEV ORF2 mAb; M. Molecular weight marker (kDa); 1. pEAQ-HT empty vector; 2. Crude extract; 3. SN (soluble protein) after extraction and spin; 4. Pellet-Insoluble part; 5. Positive control (HEV ORF2 452–617 aa recombinant protein); (c) SDS-PAGE of sucrose gradient fractions and (d) Western blot of fractions using anti-HEV ORF2 mAb; M. Molecular weight marker (kDa); 1 to 12 sucrose fractions from 10% to 60%; 13. Pellet; 14. SN after pelleting; (e) Electron microscopy of 30% (w/v) fraction and pellet.