view article

Figure 1
Expression and purification of SghA (a) and SghR (b). (a) Lane M, molecular-weight marker (labelled in kDa); lanes 1 and 2, supernatant and pellet after cell extraction, respectively; lane 3, flowthrough after Ni–NTA affinity binding; lanes 4 and 5, after elution from Ni–NTA affinity column; lane 6, purified SghA protein after gel-filtration chromatography. (b) Lane M, molecular-weight marker (labelled in kDa); lanes 1 and 2, total cells before and after IPTG induction, respectively; lane 3, flowthrough after Ni–NTA affinity binding; lanes 4 and 5, supernatant and pellet after cell extraction, respectively; lane 6, after elution from Ni–NTA purification; lane 7, purified SghR after gel-filtration chromatography.

Journal logoSTRUCTURAL BIOLOGY
COMMUNICATIONS
ISSN: 2053-230X
Follow Acta Cryst. F
Sign up for e-alerts
Follow Acta Cryst. on Twitter
Follow us on facebook
Sign up for RSS feeds