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The gels were documented by imaging with UV transillumination.
PCR products were separated on 1.5% agarose gel, and bands visualized with GelRed staining (Biotuim) and UV transillumination.
Gels were stained with RedSafe Nucleic Acid Staining Solution (iNtRON Biotechnology, Korea) and visualised by UV transillumination.
Images were documented under UV transillumination with the Gel Doc System (Bio-Rad LabOntarioes Ltd., Mississauga, Ontario).
DNA was visualized by UV transillumination.
Cell death was visualised by UV transillumination.
Amplicon size and intensity was tested on Ethidiumbromid (EtBr) stained agarose gel with UV transillumination.
All gels were stained with ethidium bromide and visualized under UV transillumination (BioRad GelDoc System, BioRad, Hercules, CA).
Amplicons were separated by 1.5% agarose gel (Fisher) electrophoresis, stained with ethidium bromide, and photographed under UV transillumination.
Finally, the gels were stained with ethidium bromide and photographed on a UV transillumination table with a CCD camera.
After amplification, the samples were separated on 2% molecular biology grade agarose gels containing ethidium bromide and bands were visualized and photographed using UV transillumination.
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