1.6.1.2	-	
1.6.1.2	affinity chromatography	
1.6.1.2	affinity chromatography on NADP+/NAD+-agarose gels, partial purification	
1.6.1.2	FPLC in the presence of 0.05 or 0.1% Triton X-100, comparison of methods	
1.6.1.2	fractionation of submitochondrial particles, DEAE-Sepharose, hydroxyapatite	
1.6.1.2	immunoexclusion chromatography	
1.6.1.2	NaCl wash, Triton X-100 extraction, affinity chromatography on immobilized NAD+	
1.6.1.2	Ni-NTA column chromatography	
1.6.1.2	Nnt is purified using an immunocapture bead matrix	
1.6.1.2	overview of early procedures	
1.6.1.2	partially purified	
1.6.1.2	recombinant domain I	
1.6.1.2	recombinant domain III	
1.6.1.2	recombinant domain III-domain I protein	
1.6.1.2	recombinant domains I and III	
1.6.1.2	recombinant enzyme	
1.6.1.2	recombinant protein	
1.6.1.2	recombinant protein using His-tag	
1.6.1.2	recombinant proteins	
1.6.1.2	soluble component