T4573

Sigma

 

Tris Acetate-EDTA buffer

working solution, Biotechnology Performance Certified

Synonym:TAE buffer
MDL number:MFCD00236357

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Description

ApplicationTAE running buffer is the most commonly used buffer for DNA agarose gel electrophoresis but is also used for non-denaturing RNA agarose gel electrophoresis.1 Double-stranded DNA tends to run faster in TAE than in other buffers but can also become exhausted during extended electrophoresis. Buffer circulation or buffer replacement during extended electrophoresis can remedy the lower buffering capacity.2 Dilution of the concentrated TAE buffer produces a 1× TAE buffer with 40 mM Tris-acetate and 1 mM EDTA, pH 8.3. The 1× TAE buffer is used both in the agarose gel and as a running buffer. Applied voltages of less than 5 V/cm (distance between the electrodes of the unit) are recommended for maximum resolution.
General descriptionSolution contains 40 mM Tris acetate and 1 mM EDTA at an approximate pH of 8.3. Made with WFI water and 0.2 μm filtered.
Preparation NotePrepared with Biotechnology Performance Certified Trizma base (T6066) and Molecular Biology Reagent EDTA disodium salt (E5134). Solutions also contain acetic acid (A6283); powdered blend contains Trizma acetate (T1258).

Properties

gradeBiotechnology Performance Certified
sterilitysterile; 0.2 μm filtered
total impurities DNase, RNase, Protease, tested
  bioburden, tested
  endotoxin, tested
 ≤5 ppm heavy metals (as Pb)
suitabilitysuitable for gel electrophoresis (after dilution to working concentration)

Safety

WGK Germany2

References

Cited Reference1. Sambrook, J., et al. Molecular Cloning: A Laboratory Manual Cold Spring Harbor, , (1989) 23, 6.7
 2. Loening, U.E., The fractionation of high-molecular-weight ribonucleic acid by polyacrylamide-gel electrophoresis. Biochem. J. 102, 251-257, (1967)
referenceOgden, R.C., and Adams, D.A., Electrophoresis in agarose and acrylamide gels. Meth. Enzymol. 152, 61-87, (1987)