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The actual liquid is a highly fluorescent neon green pigment that was lit from underneath using a UV LED system and lighting trays.
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Photoconducting characteristics of the spheres are investigated at 5 V using an UV LED (λ = 395 nm, Optical power = 400 μW).
Stimulation of bPAC was achieved using a collimated UV LED (365 nm; ∼12 mW) coupled to the epifluorescence port of the microscope (M365L2-C1; Thorland) and a TTL-controlled custom-made power supply.
The device is based on measuring the fluorescence of the chlorophyll-a (chl-a) using an UV or blue LED.
MDA is measured using the thiobarbituric acid method in which MDA, the degradation product of lipid peroxidation, condenses with penthiobarbital and leads to a red product with measurable absorbance using a UV spectrophotometer.
The chromatogram was produced using a UV Detector at 214 nm.
Fluorescence was measured using a UV spectrophotometer Xenius (Safas, Monaco) (λ = 520 nm).
It is fabricated using a UV curable low-index polymer to package a microtoroid together with its fiber-taper waveguide24,27.
Gels were viewed using a UV trans-illuminator.
The concentration of RNA was determined using a UV spectrophotometer.
The DNA was then visualized using a UV transilluminator.
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