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properties. Green fluorescent Au-NPs 1.4 nm in diameter (Alexa Fluor-488 conjugated nanogold) were purchased from Nanoprobes, Yaphank, NY, whereas CuInS/ZnS nanocrystals 3.6 nm in diameter were obtained from MK nano , Mississauga, ON, Canada. All three

R+B light, respectively ( Johkan et al., 2010 ). Similarly, salvia, petunia, and tomato seedlings grown under 50% green (G; 500–600 nm) + 50% R light from LEDs or those with ≥25% B light at the same PPF had 35% to 57% less fresh shoot weight than

verification by sequencing, the LhWDR coding sequence (CDS) fragment was cloned in front of the GREEN FLUORESCENT PROTEIN ( GFP ) sequence in a modified pCAMBIA1300 vector containing the Cauliflower mosaic virus 35S promoter and a GFP -coding region

consumers as did other genetically modified roses introducing the reporter or marker genes such as the β-glucuronidase gene, luciferase gene, neomycin phosphotransferase gene, and green fluorescent protein gene ( Firoozabady et al., 1994 ; Kim et al

., Kankakee, IL). Fig. 1. The spectral distribution of six light-quality treatments delivered by blue (B), green (G), and two types of red (R) light-emitting diodes (LEDs) and one treatment delivered by cool-white fluorescent lamps, each delivering a

image using the reflection lamp setting was taken to include the date, name, and other pertinent information for each sample. Fluorescence images were then collected using the green fluorescent protein (GFP), Texas Red (TXR), violet, and ultraviolet

light promoted stem elongation of eggplant and sunflower seedlings, and suppressed stem elongation of leaf lettuce ( Hirai et al., 2006 ) and tomato ( Li et al., 2017 ). Green LEDs increased the root dry weight of red leaf lettuce ( Johkan et al., 2012

determine impacts of supplementation on phytochemical contents in ‘Red Cross’ baby leaf lettuce. These authors showed no impacts on chlorophyll concentrations in baby lettuce when fluorescent light treatments containing 23% blue (400–500 nm)/52% green (500

triggering specific proteins in the seeds. Thus, it may be possible that the potent action of these compounds in enhancing drought acclimation may be the result of expression of a specific protein. The objectives of this study were 1) to determine if Ambiol

dsDNase (CodonX Biotechnology Co., Beijing, China). The qRT-PCR was performed with a fluorescent quantitative PCR instrument (LightCycler 480; Roche Diagnostics, Mannheim, Germany) using 2× SYBR Green qPCR Premix Universal (CodonX Biotechnology Co.). The