10X TBE Buffer Calculator

Scale a fixed 10X Tris-borate-EDTA electrophoresis buffer recipe from Tris base, boric acid, and 0.5 M EDTA solution at pH 8.0.

Select a reviewed preset and enter the final volume to prepare.

Recipe for 1 L of 10X TBE
ReagentFormulaAmount or action
Tris basefree base108 g
Boric acidanhydrous55 g
0.5 M EDTA solution, pH 8.0prepared aqueous stock40 mL
Purified waterBring the total solution volume to 1 L. Do not add 1 L of water; add water only until the total solution reaches 1 L.

How to prepare 10X TBE

  1. Add the calculated Tris base and boric acid to approximately 70–80% of the selected final volume of purified water.
  2. Stir until both solids dissolve completely.
  3. Add the calculated volume of 0.5 M EDTA solution, pH 8.0 and mix thoroughly.
  4. Bring to the selected final volume with purified water.

About This Buffer

TBE, or Tris-borate-EDTA, is widely used for nucleic acid electrophoresis in agarose and polyacrylamide gels. It uses borate rather than acetate as part of the buffer system. This page scales a fixed 10X TBE stock prepared from Tris base, boric acid, and a source-defined 0.5 M EDTA solution at pH 8.0; the reviewed preset does not specify a separate final-stock pH adjustment.

Common questions

Is the 10X TBE stock pH adjusted?

This fixed preset contains no separate pH-adjustment operation. It is prepared from the listed components and brought to volume.

How do I prepare 1X TBE from 10X stock?

Use a 1:10 dilution of the completed 10X stock when a protocol calls for 1X TBE.

How is TBE different from TAE on ChemH?

TBE uses boric acid and is published as a 10X stock, while TAE uses glacial acetic acid and is published as a 50X stock.

Sources and review notes

The source for the currently selected preset appears first. Recipe quantities remain tied to the cited article location.