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. 2012 Jan 23;7(1):e30499. doi: 10.1371/journal.pone.0030499

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López-Garrido, Casadesús.

This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.

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A. ß-galactosidase activity of STM3026::lac, STM3025.1N::lac, and STM3025::lac translational fusions in a Dam⁺ background (black histograms) and in a Dam⁻ background (white histograms). ß-galactosidase activity has been relativized to 100 in the Dam⁻ background. Student's t test indicates that the differences observed in the ß-galactosidase activities of the fusions in a Dam⁺ and Dam⁻ backgrounds are statistically significant (P<0.005 in every case). B. Levels of STM3026 (StdD), STM3025.1N (StdE), and STM3025 (StdF) proteins in extracts from Dam⁺ and Dam⁻ hosts. 3xFLAG-tagged proteins were detected by Western blotting using anti-FLAG antibodies. GroEL was used as loading control. For quantification, the ratio tagged protein/GroEL was relativized to 100 in the Dam⁻ background.