EC Number |
---|
3.4.11.21 | 2000fold to homogeneity, Triton X-100 solubilized microsomal fraction, DEAE-cellulose chromatography, immunoadsorbent chromatography |
3.4.11.21 | 722fold near homogeneity by conventional chromatography techniques |
3.4.11.21 | aspartyl aminopeptidase is purified from yeast cells, using ultracentrifugation, ammonium sulfate fractionating, and chromatography on a Bio-Gel column, on a Mono Q column, and a Superose 6 column |
3.4.11.21 | DEAE-Sephacel gel filtration and TSK phenyl 5-PW gel filtration |
3.4.11.21 | native enzyme 454.5fold from koji by ammonium sulfate fractionation, dialysis, and ultrafiltration, followed by affinity and anion exchange chromatography, another step of ammonium sulfate fractionation, and gel filtration |
3.4.11.21 | native enzyme to homogeneity by ultracentrifugation, ammonium sulfate fractionation, anion exchange chromatography, and gel filtration |
3.4.11.21 | Ni-NTA-agarose column chromatography and Superdex-200 gel filtration |
3.4.11.21 | Ni-Sepharose 6 Fast Flow column chromatography |
3.4.11.21 | non-fusion protein expressed in Escherichia coli, 440fold to homogeneity |
3.4.11.21 | partial, ammonium sulfate fractionation, gel filtration, ion-exchange chromatography |