2.3.4. Agarose Gel ELECTROPHOSIS<br>PCR products were checked in 1.2% agarose gels prepared in 0.5X TBE buffer containing 0.5 sg/ml ethidium bromide. 1 sl of 6X load edd dye mixed with 5 sl of PCR products, was-loaded and was-loaded and an-phosis performed with 0.5X TBE buffer for 1-hours, until the bromo thebromol blue front to migrated to the bottom of the forthe gel. The molecular standard used was 2-log DNA<br>ladder (NEB). The gel ag edd in a UV transror (Genei) and the image was captured under UV light gyda sgoil yn sylweddol . ...
正在翻譯中..
