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The Cold-Active TEV Protease recognition sequence with the highest catalytic efficiency is ENLYFQ ▼S; however, the amino acid in the P1’ position can also be G, A, M, C, H or F.
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Cold-Active TEV Protease is suitable for use from 4°C to 37°C.
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Reactions may be scaled up linearly to accommodate larger reaction volumes.
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We recommend dialyzing the fusion protein before Cold-Active TEV Protease treatment if the fusion protein is in a buffer containing > 2 M urea, > 1 M Guanidine hydrochloride, > 30% glycerol, pH below 6 or above 9, or cysteine protease inhibitors.
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Cold-Active TEV Protease is a cysteine protease and is compatible with the following protease inhibitors: aprotinin, benzamidine, leupeptin, pepstatin, PMSF.
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Buffer and reagents compatibility tested with Cold-Active TEV Protease:
| Buffer/Additives |
Activity >80% |
Activity >50% |
Not recommended |
| HEPES 10 mM |
pH 7 to 10 |
- |
- |
| Tris 50 mM |
pH 7 to 9 |
- |
- |
| Potassium Phosphate 50 mM |
pH 6 to 8 |
- |
- |
| Sodium phosphate 100 mM |
pH 6 to 8 |
- |
- |
| Sodium Acetate 50 mM |
pH 5.5 |
- |
pH 4.5 |
| PBS/NEBExpress E. coli lysis reagent (NEB #P8116) |
1x |
- |
- |
| NaCl |
500 mM |
Tested up to 2 M |
- |
| KCl |
Tested up to 200 mM |
- |
- |
| CaCl2 |
Tested up to 20 mM |
- |
- |
| MgCl2 |
Tested up to 10 mM |
- |
- |
| MnCl2 |
Tested up to 10 mM |
- |
- |
| ZnSO4 |
1 mM |
- |
>1 mM |
| Glycerol |
10% |
Tested up to 30% |
- |
| Imidazole |
Tested up to 500 mM |
- |
- |
| EDTA |
10 mM |
Tested up to 100 mM |
- |
| DTT |
Tested up to 20 mM |
- |
- |
| Tween 20 |
Tested up to 0.5% |
- |
- |
| Triton X-100 |
Tested up to 1% |
- |
- |
| SDS |
- |
- |
Tested 0.01% to 5% |
| Urea |
1 M |
3 M |
3 to 6 M |
| Guanidine Hydrochloride |
3 M |
- |
3 to 6 M |
References
1. Kapust, R.B. et al. (2002). Biochem. and Biophysical Research Comm. 294, 949-955.