EC Number   |
|---|
   5.6.1.5 | M2 agarose affinity column chromatography |
| 5.6.1.5 | Mpa fragments are purified as N-terminal fusions with His6-tagged maltose-binding protein followed by a TEV cleavage site, producing the folowing fragments: Mpa-wt (residues 1-609), Mpa-CC (residues 1-98), Mpa-ID (99-216), and Mpa-CC-ID (1-216) |
| 5.6.1.5 | NeutrAvidin agarose column chromatography and Superose 6 gel filtration |
| 5.6.1.5 | NeutrAvidin agarose resin column chromatography and Superose 6 gel filtration |
| 5.6.1.5 | NeutrAvidin agarose resin column chromatography, and Superose 6 gel filtration |
| 5.6.1.5 | Ni-NTA column chromatography and Superdex 200 gel filtration |
| 5.6.1.5 | proteasomes are prepared from rabbit reticulocyte lysates |
| 5.6.1.5 | proteins are extracted from heart tissue |
| 5.6.1.5 | proteins are extracted from pupae and larvae of Drosophila melanogaster |
| 5.6.1.5 | purified in the presence of ATP-gammaS and ATP |
