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The pDNA bands were then visualized using a UV transilluminator at 365 nm.
RNA or DNA bands were visualized using a UV transilluminator and immediately photographed.
The PCR product was electrophoresed on a 2% TAB agarose gel for 1 hour at 70V and the bands were analyzed using a UV transilluminator.
Similarly, 50 µl of the same cell-free supernatants were applied five times into 4-mm holes in rhodamine B agar plates [64], and the plates were imaged using a UV transilluminator after incubation at 37°C for 3 days to visualize lipase activity.
The products were visualized using a UV transilluminator.
The DNA was then visualized using a UV transilluminator.
Similar(30)
Nucleic acids were detected using an UV transilluminator (BioRad, Hercules, CA, USA).
The gels were stained with 0.5 μg mL-1 ethidium bromide, visualised using an UV transilluminator and then photographed.
Heteroduplex products were separated using 6% non-denaturating polyacrylamide electrophoresis in 0.5× TBE-buffer, stained with 0.5 µg/ml ethidium bromide, and visualised using a UV-transilluminator.
The gels were stained (8 μl of 10 mg/ml ethidium bromide in 200 ml 1× TAE buffer) for ∼7 minutes and the stained bands were visualized using an UV-transilluminator (ATTO, Tokyo, Japan).
PCR products were visualized on 1.2% (w/v) agarose gels using a UV light transilluminator.
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