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50x TAE Electrophoresis Buffer - University of California ...
Disodium EDTA 18.61 g Glacial Acetic Acid 57.1 ml DDI H2O to 1 l Add the Tris free base and EDTA to approximately 700 ml DDI H2O and stir until the Tris and EDTA are dissolved. Add the acetic acid and adjust the volume to 1 liter. The 1x TAE solution is 40mM Tris, 20mM Acetate and 1mM EDTA and typically has a pH around 8.6 (do not adjust).
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microbiology.ucdavis.eduAug 18, 2003 · 3] Pour the resolving gel mixture into the gel plates to a level 2 cm below the top of the shorter plate. 4] Pace a layer of DDI H 2O over the top of the resolving gel to prevent meniscus formation in the resolving gel. 5] Allow resolving gel to stand 30 min at room temperature. 6] Drain the DDI H 2O from top of the resolving gel. Rinse with DDI H
DNA Polyacrylamide Gel Electrophoresis
microbiology.ucdavis.edu5x TBE electrophoresis buffer Polyacrylamide gels are poured and run in 0.5x or 1x TBE at low voltage (1-8 V/cm) to prevent denaturation of small fragments of DNA by heating. Other electrophoresis buffers such as 1x TAE can be used, but they are not as good as TBE. The gel must be run more slowly in 1x TAE, which does not provide as
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