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. 2017 Feb 16;12(2):e0172445. doi: 10.1371/journal.pone.0172445

Fig 1. Purification of natively folded SEA, SEE and SEH.

Fig 1

(A, C, E) Size-exclusion chromatography of SEA, SEE and SEH, with protein purities analyzed by coomassie-stained SDS-PAGE gels shown as insets. (B, D, F) Far-UV CD spectra for SEA, SEE, SEH at 200–250 nm at 20°C in presence of 0.1 mM ZnCl2 (dark grey) or 1 mM EDTA (light grey) at pH 6.0.