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. 2018 Nov 1;13(11):e0206813. doi: 10.1371/journal.pone.0206813

Fig 4.

Fig 4

Oligomeric structure of Vip3Aa65 protoxin and trypsin-activated toxin under native (A) and denaturing (B) conditions. A) Gel filtration chromatography in a Superdex 200 10/30 GL column. B) SDS-PAGE analysis of the 12 ml peak from the protoxin (P) and the activated toxin (A). M: Molecular weight markers in kDa.