2.3.1.255	HisTrap column chromatography and Superdex 75 gel filtration	
2.3.1.255	Ni-NTA resin column chromatography and Superdex 200 gel filtration	
2.3.1.255	Ni-NTA resin column chromatography, Q ion exchange column chromatography, and S200 gel filtration	
2.3.1.255	Ni-Sepharose column chromatography and Sephacryl S-200 gel filtration	
2.3.1.255	recombinant C-terminally His6-tagged enzyme RimI from Escherichia coli by nickel affinity and gel filtration	
2.3.1.255	recombinant GST-tagged wild-type and mutant Naa10 enzymes from Escherichia coli strain BL21 by glutathione affinity chromatography	
2.3.1.255	recombinant His-MBP-tagged wild-type and mutant Naa10 from Escherichia coli strain BL21 Star DE3 by affinity chromatography	
2.3.1.255	recombinant His-tagged and maltose binding protein-tagged subunits hNaa15p, hNaa10p, and hNaa50p from Escherichia coli by nickel affinity chromatography	
2.3.1.255	recombinant His-tagged ARD1/Naa10 from Escherichia coli by nickel affinity chromatography, anion exchange chromatography, and gel filtration. After purification, rhARD1/NAA10 mainly exists in a high oligomeric state and has only a few monomers. Recombinant GST-tagged enzyme from Escherichia coli strain BL21 by glutathione affinity chromatography	
2.3.1.255	recombinant His-tagged enzyme from Escherichia coli strain BL21(DE3) by nickel affinity chromatography and gel filtration	
2.3.1.255	recombinant His-tagged hARD1/NAA10 enzyme by nickel affinity chromatography, with or without anion exchange chromatography, followed by gel filtration, and dialysis, rhARD1/NAA10 aggregates during purification	
2.3.1.255	recombinant His-tagged hNatA by affinity chromatography and gel filtration	
2.3.1.255	Resource Q column chromatography, Mono Q column chromatography, and Superdex 200 gel filtration	
2.3.1.255	ribosomes of HEK-293 cells are isolated