These gels are suitable for separating nucleic acids, giving sharp DNA bands and low background fluorescence. DNase activity and DNA binding are not detected. The gels are cast using a 1x TBE (0.089 M Tris-borate, pH ~8.3, containing 2 mM EDTA) buffer system with ethidium bromide (0.5 µg/mL) included in the gel for easy visualization.
Tray dimension: 6.8 cm x 10.2 cm
Gel dimension: 6.0 cm x 9.5 cm
Gel thickness: 5.5 mm
Precast Agarose gels require less than 5 minutes to set up.
Dye Migration with 1x TBE
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