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The basics. Agarose gels can be used to resolve large fragments of DNA. Polyacrylamide gels are used to separate shorter nucleic acids, generally in the range of 1−1000 base pairs, based on the concentration used (Figure 1). These gels can be
Gel loading buffer: To make 10 mL of 4X stock: 2.0 ml 1M Tris-HCl pH 6.8. 0.8 g SDS. 4.0 ml 100% glycerol. 0.4 ml 14.7 M β-mercaptoethanol. 1.0 ml 0.5 M EDTA. 8 mg bromophenol Blue. Staining solution: Weigh 0.25g of Coomassie Brilliant Blue R250
