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. 2012 Oct 19;6:79–87. doi: 10.2174/1874285801206010079

Fig. (2).

Fig. (2)

Analysis of purified recombinant proteins by metal chelating chromatography through SDS-12% PAGE. Purified protein eluted from Ni+2 - charged chelating sepharose column with 1 M imidazole. Lane M, molecular mass protein marker; lane 1, rLIC10821 (37 kDa); lane 2, Lsa66 (65 kDa); lane 3, Lsa25 (24 kDa); lane 4, Lsa21 (21 kDa); lane 5, rLIC11030 (37 kDa); lane 6, rLIC10672 (23 kDa). Protein bands were visualized by Coomassie blue staining. Positions of molecular mass standards are indicated on the left (in kDa). (*) denotes each protein band.