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. 2019 Mar 4;9:3359. doi: 10.1038/s41598-019-40044-4

Figure 6.

Figure 6

Purification of SBP-tagged β-lactamase using M18-L-DBD affinity matrix under a non-overloading condition. (a) Analysis of different fractions from the column by SDS-PAGE. S, B. subtilis culture supernatant containing overproduced SBP-tagged β-lactamase; FT, flow-through fraction; W, wash fractions; E, elution fractions. Open arrowhead indicates SBP-tagged β-lactamase. (b) SDS-PAGE of the bound fraction from the M18-L-DBD Sephadex column used for purification of SBP-tagged β-lactamase. Lane 1 is the boiled matrix before sample loading; lane 2 represents the boiled matrix after sample loading and before elution with biotin; lane 3 is the boiled matrix after elution with biotin. Closed arrowhead, M18-L-DBD; Open arrowhead, retained SBP-tagged β-lactamase. M, molecular weight markers (sizes in kDa). Gel profiles shown in panels a and b are from different gels.