T9525-1GA Display Image

Tris-Borate-EDTA buffer, working solution

Code: T9525-1GA D2-231

Application

TBE running buffer is the most commonly used buffer for DNA and RNA polyacrylamide gel electrophoresis. TBE is used with non-denaturing or denaturing (...


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Application

TBE running buffer is the most commonly used buffer for DNA and RNA polyacrylamide gel electrophoresis. TBE is used with non-denaturing or denaturing (7 M urea) gels. It is also routinely used for DNA automated sequencing gel. TBE can also be used for agarose gels but is not recommended for preparative gels for recovery of nucleic acids. Dilution of the TBE stock concentrates to a 1× TBE running buffer results in a buffer containing 89 mM Tris-borate and 2 mM EDTA, pH 8.3. The 5× or 10× stocks may also be added to an acrylamide/bis-acrylamide stock solution for making the PAGE gel. Applied voltages of less than 5 V/cm (distance between the electrodes of the unit) are recommended for maximum resolution.

Other Notes

89 mM Tris borate, pH approx. 8.3, containing 2 mM EDTA.

Packaging

Supplied in dispenser with a spigot.

Preparation Note

Prepared with Biotechnology Performance Certified Trizma base (Product Code T6066) and Molecular Biology Reagents boric acid (Product Code B6768) and EDTA disodium salt (Product Code E5134).

Solution prepared with 18 megohm water

application(s)diagnostic assay manufacturing
formworking solution
impuritiesDNase, RNase, Protease, none detected
InChI keyOSBLTNPMIGYQGY-UHFFFAOYSA-N
InChI1S/C10H16N2O8.C4H11NO3.BH3O3/c13-7(14)3-11(4-8(15)16)1-2-12(5-9(17)18)6-10(19)20;5-4(1-6,2-7)3-8;2-1(3)4/h1-6H2,(H,13,14)(H,15,16)(H,17,18)(H,19,20);6-8H,1-3,5H2;2-4H
Quality Level200
SMILES stringOB(O)O.NC(CO)(CO)CO.OC(=O)CN(CCN(CC(O)=O)CC(O)=O)CC(O)=O
sterility0.2 µm filtered
suitabilitysuitable for gel electrophoresis (after dilution to working concentration)
technique(s)electrophoresis: suitable
This product has met the following criteria: