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. 2015 May 5;10(5):e0125229. doi: 10.1371/journal.pone.0125229

Fig 3. Purification of recombinant ClIDH.

Fig 3

(a) Protein purity was assessed via 12% SDS-PAGE. M, protein marker; lane 1, crude extracts of cells harboring pET-28b(+) after induction with IPTG; lane 2, crude extracts of cells harboring the recombinant plasmid after induction with IPTG; lane 3, purified protein. (b) Western blot analysis using the anti-6×His antibody as a probe. Lane 1, negative control, crude extracts of cells harboring pET-28b(+) with IPTG induction; lane 2, purified protein. (c) Molecular mass determination via gel filtration chromatography. The Ve of recombinant ClIDH was 10.7 mL.