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Both the cuvettes and the caps were sterilized prior to use using a UV germicidal lamp.
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The plates were exposed to germicidal UV radiation using a UV tube light (Sankyo Denki Co. Ltd., Japan) at 10 cm height, for 3 12 s and incubated in dark, at 28 °C, for 5 7 days.
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.
DNA was visualized using a UV transilluminator and photographed.
The UV power output was measured using a UV light meter with a peak sensitivity at 340 nm (LUYOR, UV 340B, China).
The drug content was determined using a UV method.
For a DSLR, consider using a UV filter.
Sections were observed using a UV-fluorescence microscope.
The RNA was UV cross-linked to the membrane using a UV-light (GS Gene linker, BioRad).
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