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. 2015 Jul 28;71(Pt 8):993–997. doi: 10.1107/S2053230X15010195

Figure 1.

Figure 1

(a) Size-exclusion chromatography trace of recombinant galectin-1118–140. Arrows indicate the elution volumes of proteins of known molecular weight (labelled in kDa). (b) SDS–PAGE analysis of purified protease-treated recombinant galectin-1118–140 (lane 2). Molecular weights (lane 1) are indicated on the left in kDa. (c) Recombinant galectin-111–140 is shown to be functional by elution from a galactose Sepharose column with different sugars. Lanes 2, 3, 4 and 5 show galectin-111–140 eluted from a column with galactose, lactose, mannose and fructose, respectively. The positions of molecular-weight markers (labelled in kDa) are shown in lane 1.