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. 2013 Aug 28;54:22. doi: 10.1186/1999-3110-54-22

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© Lin et al.; licensee Springer. 2013

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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Validation of the infectivity of pBD-TuMV-CY5, pBD-TuMV-GFP and pBD-TuMV-GK on N. benthamiana plants. The agro-infiltrated N. benthaminana plants were analyzed with western blotting (A) or indirect ELISA (B) at 7 dpi, using the antiserum to TuMV CP. The samples of agro-infiltrated leaves are individually indicated. The sample from leaves infected by TuMV virus culture (14 dpi) that was used as positive control is indicated as TuMV. The mock was inoculation was used as a negative control. The blank indicates the wells coated with buffer for basal-level control. The TuMV CP antiserum was used at 10,000x dilution for both assays. The samples significantly different with mock (p-value < 0.05) were indicated as “*”. Bars represent standard deviations (n = 3).