EC Number |
Reference |
---|
3.4.21.72 | - |
37007, 651233, 666398, 666834, 710668 |
3.4.21.72 | development and evaluation of a method for isolation and purification of IgA1 protease from a culture of Neisseria meningitidis serogroup A, purification involves absorption, hydrophobic interaction, anion exchange, and jacalin affinity chromatography steps, to homogeneity, overview |
718393 |
3.4.21.72 | native enzyme by hydrophobic interaction chromatography, ultrafiltration, anion exchange chromatography, dialysis, gel filtration, and again ultrafiltration |
755437 |
3.4.21.72 | native enzyme from three inactivated intermediates of meningococcal vaccine production |
717322 |
3.4.21.72 | Ni-NTA agarose column chromatography |
712742 |
3.4.21.72 | recombinant extracellular His6-tagged IgA protease from Escherichia coli culture medium by nickel affinity chromatography, dialysis, and ultrafiltration, to over 95% purity |
754698 |
3.4.21.72 | recombinant His-tagged enzyme variants solubilized from Escherichia coli inclusion bodies by nickel affinity chromatography, dialysis, and anion exchange chromatography |
753131 |
3.4.21.72 | recombinant His-tagged IgA1 protease by nickel affinity chromatography, anion exchange chromatography, and gel filtration |
717879 |
3.4.21.72 | recombinant isolated surface-exposed SD domain from Escherichia coli to homogeneity |
717170 |
3.4.21.72 | recombinant refolded enzyme solubilized from Escherichia coli inclusion bodies by ion exchange and hydrophobic interaction chromatography, followed by ultrafiltration and diafiltration |
753982 |