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Fastgene blue green led flashlight

Manufactured by Nippon Genetics
Sourced in Germany, Japan

The FastGene® Blue/Green LED Flashlight is a compact, battery-powered device that emits blue or green light. It is designed for use in laboratory settings.

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2 protocols using fastgene blue green led flashlight

1

Tracking E. coli GFP in rhizotrons

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We used a fluorescent and nonpathogenic strain E. coli GFP ATCC® 25922GFP™ (American Type Culture Collection, Manassas, VA, USA). It harbors a multicopy vector encoding the green fluorescent protein GFPmut3. The GFPmut3 fluorophore has an excitation maximum at 501 nm and an emission maximum at 511 nm, compatible with usual fluorescence detection technologies. The plasmid-borne bla gene confers the resistance to 100 µg/mL of ampicillin. This E. coli strain has been grown in a Luria-Bertrani (LB) broth overnight at 37 °C with gentle shaking to reach the growth plateau (~109 CFU/mL). Then, an aliquot of the culture of 6 mL with a concentration of 2.4 × 106 CFU/mL was inoculated in rhizotrons via a sterile pipette for water inoculation and via sterile syringe connected to a tube to reach a 5-cm depth in sediments to simulate contaminations from the surface water and groundwater, respectively. To make the strain visible, it was excited at each measure by lightening the rhizotrons with a FastGene® Blue/Green LED Flashlight (Nippon Genetics Europe GmbH, Dueren, Germany) emitting at 480–530 nm.
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2

Visualizing GFP Expression in Agroinjected Plants

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GFP fluorescence was verified with a FastGene ® blue/green LED flashlight (FG-11; NIPPON Genetics, Tokyo, Japan), which was used to irradiate (excitation: 489 nm; emission: 520 nm) leaves and fruit at the mature red ripening stage (about three days after agroinjection) at a distance of ~ 10 cm from each organ in the dark. To photograph the irradiated leaves, a yellow UV filter (NIPPON Genetics) was mounted to the camera (Nikon Coolpix B500, Tokyo, Japan) lens to filter out blue light, and to allow GFP fluorescence to be visualized. Fluorescence was also verified in controls at the same time. The location of GFP fluorescence was visually assessed and confirmed. Three controls were used for both methods at the same time as the agroinjection into ripe fruits and leaves using infiltration solution: (a) without any A. tumefaciens; (b) A. tumefaciens without any plasmid; (c) A. tumefaciens with a constitutive promoter (CaMV-35S) + sGFP in the plasmid.
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