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Products: Eznyme Toolbox: TurboTEV

TurboTEVTM Protease

Catalog #: Size: Concentration: Price:
T0102M 1 mg (10,000 Units) 2 mg/ml $489
T0102L 10 mg (100,000 Units) 2 mg/ml $4,160
T0102B Bulk 2 mg/ml Inquiry

To Order: Please email PO to or fax PO to 888-239-6490

Cleavage in Solution
  1. Make fresh cold Dialysis Buffer. Dialysis Buffer should be a buffer in which the target protein is soluble. There should be no protease inhibitor in the Dialysis Buffer. The Dialysis Buffer should be compatible with downstream purification processes, e.g. minimal amount of EDTA or DTT if Ni column will be used to remove the cleaved His-tag.

    Here is an example of Dialysis Buffer. 25 mM Tris-HCl, pH 8.0, 150 - 500 mM NaCl, 14 mM b-mercaptoethanol

    TurboTEV has the same activity in 150 mM NaCl or 500 mM NaCl and 400 mM imidazole.

  2. Dilute the target protein pool to 1-2 mg/ml with Dialysis Buffer. This is optional in case the target protein aggregates in Dialysis Buffer. Save a small aliquot as Uncut sample for analysis. EDTA may be added to 0.5 mM final concentration if the target protein pool is eluted from Ni column and EDTA is compatible with the target protein.

  3. Add TurboTEV Protease at a Protease:target protein ratio of 1:100 (w/w) or 10,000 unit (1 mg) TurboTEV Protease to 100 mg of target protein. There is no need to calculate the molar ratio. TurboTEV Protease can be added directly to the target protein. There is no need to change buffer or dilute TurboTEV Protease. The optimal ratio should be determined empirically. A Protease-to-target protein ratio (w/w) of 1:50 to 1:200 should work for most target proteins.

  4. Dialyze against the Dialysis Buffer at 4oC overnight (about 16 hrs). Dialysis is to remove imidazole or glutathione if Ni or glutathione column is used to remove the cleaved tag or TurboTEV Protease after cleavage. If desired, the target protein pool can be buffer exchanged first before TurboTEV cleavage.

Removal of TurboTEV Protease
  1. The dialyzed target protein and TurboTEV Protease mixture can be applied directly to affinity columns if compatible Dialysis Buffer is used. For His-tagged protein, use IMAC to remove the cleaved His-tag and TurboTEV Protease. For GST-tagged protein, use glutathione column to remove the cleaved GST-tag and TurboTEV Protease.

  2. If desired, analyze samples using SDS-PAGE analysis. The difference between the tagged and cleaved target protein may be too small to detect by SDS-PAGE. The cleaved His-tag sometimes can be seen at the bottom of the gel.

US Distributors:
Fisher Scientific
Eton Bioscience
A.G. Scientific
International Distributors:
Nacalai Tesque in Japan
MoBiTec in Europe

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