This protocol describes the resolution of genomic DNA by TAFE, followed by blotting and hybridization. 1 | Cast a 1% agarose gel in 1× TAFE gel buffer (20 mM Tris-acetate (pH 8.2), 0.5 mM EDTA ...

Gel electrophoresis is a laboratory method used to separate mixtures of DNA, RNA, or proteins according to molecular size. In gel electrophoresis, the molecules to be separated are pushed by an ...

In combination with EMBER™ DNA Loading Dye or EMBER™ Ultra RNA Loading Dye, this system supports RNA and DNA agarose gels between 1% and 5%, and does not require post-electrophoresis staining for fast ...

With an E-Gel ® iBase™ Power System, separation of DNA can typically be completed in just 7 minutes, perfect for quick analysis of your DNA fragment prior to downstream applications.