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Separated DNA fragments (DNA ladders) were visualized using a UV trans-illuminator (310 nm).
Gels were viewed using a UV trans-illuminator.
Gels were stained with ethidium bromide and viewed using a UV trans-illuminator.
Reactions were resolved on 2% agarose gels that were stained with ethidium bromide and viewed using a UV trans-illuminator.
PCR products were then separated by electrophoresis in 1.5% agarose gels with 1XTAE running buffer at 8V/cm for 70 minutes and stained with Ethidium bromide (0.5µg/ml), (Sigma Aldrich), for 30 minutes and visualized using a UV trans-illuminator.
The amplification products were analysed by electrophoresis through a 1.5% agarose gel containing 1× TBE and 0.5 μg/ml ethidium bromide and visualised using a UV trans-illuminator (Ultra-Violet Products).
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The digested fragments of dCAPS markers and amplicons of other markers stained by ethidium bromide were visualized on a UV trans-illuminator after electrophoresis using 9% non-denaturing polyacrylamide gels or 1% agarose gels depending on fragment size.
PCR products were analyzed using 1% agarose gel electrophoresis and visualized on a UV trans-illuminator after ethidium bromide staining.
The products were analyzed using 9% non-denaturing polyacrylamide gel electrophoresis and visualized on a UV trans-illuminator after ethidium bromide staining.
Gels were stained with ethidium bromide, visualized and photographed on a UV trans-illuminator (Vilber Lourmat, QUANTUM ST4).
Following electrophoresis, gels were stained with ethidium bromide and viewed on a UV trans-illuminator (FirstLight UVP, San Gabriel, CA, USA).
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