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DNA banding patterns were visualized under UV light with ethidium bromide staining.
Banding patterns were visualized by ethidium bromide staining and photodocumented under UV light.
DNA banding patterns were visualized with 0.1% ethidium bromide and digitally photographed.
DNA banding patterns were visualized on a UV-transilluminator (Sigma) after staining for 15 min in ethidium bromide (20 μg/ml) and destaining for 5 min in H2Obidest.
Subsequent to development, the banding patterns were visualized in 254 nm, 366 nm and white light and the Rf values were calculated.
5.0 μg of each of DNA samples were resolved by electrophoresis for 4 h on a 1.5% agarose gel and stained with ethidium bromide and the banding patterns were visualized with the Foto/Eclipse UV transilluminator.
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The obtained band patterns were visualized by mean of gel electrophoresis and analysed by using the free software gelAnalyser (http://www.gelanalyzer.com).
After PFGE, the band patterns were visualized by ethidium bromide staining and then photographed (GelDoc™ imaging system, Bio-Rad, Munich).
Band patterns were visualized with a silver staining method [ 54].
After gel electrophoresis, band patterns were visualized with silver staining, and gel images were taken with a digital camera.
After reaction, MSSCP analysis was performed and ssDNA band patterns were visualized as presented in Figures 3 and 4. The presence of all Australian genetic variants was clearly detected in combinations with each other and with vaccine Roakin strain.
More suggestions(16)
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banding patterns were matched
banding patterns were compared
banding patterns were sequenced
banding patterns were called
banding patterns were reconstituted
banding patterns were considered
banding patterns were evaluated
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