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. 2010 Nov 1;7(6):796–802. doi: 10.4161/rna.7.6.13768

Figure 1.

Figure 1

Steady-state levels of RpoS determined by quantitative western-blotting in the wt strain and the isogenic csdA mutant. The E. coli strains WJW45 (wt), the isogenic csdA deficient strain WJW45ΔcsdA (csdA) as well as WJW45ΔcsdA harbouring plasmid pUCdeaD38 (csdA/pUCdeaD) were grown to early log phase (OD600 of 0.4) either at 37°C (lane 2–4) or at 24°C (lane 5–7), respectively. Cell extracts of the rpoS mutant strain RH90,53 served as a negative control (lane 1). Equal amounts of total cellular proteins were loaded in each lane of the SDS-polyacrylamide gel. The RpoS protein was detected by immunological means as described in Materials and Methods. Only the relevant section of the immunoblot is shown.