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. 2018 Oct 10;19(1):foy112. doi: 10.1093/femsyr/foy112

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© FEMS 2018.

This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.

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Figure 2. — Bacterial expression and purification of CaPho15p (A) and CpPho15p (B). SDS-PAGE shows the protein composition of cell lysate (lane 1), soluble cytoplasmic fraction (lane 2), wash of the inclusion bodies (lane 3), inclusion bodies (lane 4), solubilised inclusion bodies after dialysis (lane 5), flow-through fraction after His-tagged protein binding to Ni-NTA Agarose (lane 6), wash of the column (lane 7), purified phosphatase (lane 8). M—Molecular weight marker.