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. 2007 May 12;63(Pt 6):512–515. doi: 10.1107/S1744309107022154

Figure 1.

Figure 1

SDS–PAGE showing fractions purified by Ni–NTA and gel-filtration chromatography. Proteins were separated on 12% SDS–PAGE and stained with Coomassie Brilliant Blue. Lane 1, molecular-weight markers (kDa); lanes 2–4, Ni–NTA purified fractions; lanes 5–6, gel-filtration purified fractions.