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. Author manuscript; available in PMC: 2018 Apr 9.
Published in final edited form as: FEBS J. 2010 Jun;277(12):2654–2662. doi: 10.1111/j.1742-464X.2010.07675.x

Figure 1. Protein purification.

Figure 1

Coomassie-stained denaturing gels of purified MBP-NBDs (A) and full-length SUR2A (B), SUR2B (C). Numbers adjacent to the gel indicate the molecular weights (mw, kDa). (A) Lanes: 1=NBD2A; 2=NBD2B; 3=NBD1; 4, mw markers. (B) Lanes: 1=SUR2A; 2, mw markers. (C) Lanes: 1, mw markers; Lane 2=SUR2B. Samples are purified eluates from affinity resins without further purification (A) or eluates from the gel filtration column (B, C).