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. 1998 Dec 8;95(25):15123–15128. doi: 10.1073/pnas.95.25.15123

Figure 1.

Figure 1

Purification of rGSII and its mutant forms by Ni2+ chelate affinity chromatography. Transformed host E. coli strain BL21 (DE3) cells were used for recombinant protein production, followed by protein purification with a Ni2+ chelate affinity column (Novagen).