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. 2018 Jun 12;8:8952. doi: 10.1038/s41598-018-27433-x

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© The Author(s) 2018

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

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Incorporation of the SIV gp160 into rNDV particles. The allantoic fluid containing each virus was harvested from eggs and passed through 30% sucrose cushion. The sedimented virus was suspended in PBS and used for Western blot analysis. Monoclonal antibodies specific to SIV gp160 and NDV HN were used to detect these proteins. Molecular weight of the detected virus proteins (in kDa) are shown.