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Catalog Number | Quantity |
---|---|
B52 | 1 L |
A TAE running buffer used in conjunction with a TBE gel would create high current and may lead to gel hydrolysis. Also, the acetate ion in TAE migrates faster than the borate ion in TBE buffer, and can create fuzzy bands. It is possible to try soaking the TBE gel (run in TBE buffer) in the TAE buffer following the run and then eluting from that. Since nucleic acids diffuse out of the gel relatively slowly, this may work.
Find additional tips, troubleshooting help, and resources within our Nucleic Acid Purification and Analysis Support Center.
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