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. 2018 Jul 6;19(7):1969. doi: 10.3390/ijms19071969

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© 2018 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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Evaluation of the CvpsaD promoter function in higher plants. Green fluorescent protein (GFP) analysis and the β-glucuronidase (GUS) histochemical assay were performed on the infiltrated leaves. (a) Schematic representation of promoter cassettes conjugated with the GFP-GUS fusion gene. (b) Green fluorescence in epidermal cells and (c) GUS reporter assay in leaf tissue of N. benthamiana. Transient expression of GFP-GUS three days after infiltration with Agrobacterium harboring GFP-GUS vector.

Evaluation of the CvpsaD promoter function in higher plants. Green fluorescent protein (GFP) analysis and the β-glucuronidase (GUS) histochemical assay were performed on the infiltrated leaves. (a) Schematic representation of promoter cassettes conjugated with the GFP-GUS fusion gene. (b) Green fluorescence in epidermal cells and (c) GUS reporter assay in leaf tissue of N. benthamiana. Transient expression of GFP-GUS three days after infiltration with Agrobacterium harboring GFP-GUS vector.