File:Characterization of RBS* performed by Heidorn et al 2011.gif

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“Comparison of four different ribosome binding sites BBa_B0030, BBa_B0032, BBa_B0034 (Registry of Standard Biological Parts), and RBS* in Escherichia coliDH5α (white bars) and Synechocystis PCC 6803 (black bars). The translational efficiencies were measured by means of GFPmut3B fluorescence and divided by the absorbance of the cultures at 595 nm (E. coli) or 750 nm (Synechocystis), respectively. The data represent mean ± S.D. of 4 measurements each of three independent cultivations.” Figure and figure description are taken from: Heidorn, T., Camsund, D., Huang, H. H., Lindberg, P., Oliveira, P., Stensjo, K., & Lindblad, P. (2011). Synthetic biology in cyanobacteria engineering and analyzing novel functions. Methods Enzymol, 497, 539-579. doi: 10.1016/B978-0-12-385075-1.00024-X

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current18:23, 9 October 2016Thumbnail for version as of 18:23, 9 October 2016401 × 252 (6 KB)Marangiop (Talk | contribs)
18:20, 9 October 2016Thumbnail for version as of 18:20, 9 October 2016401 × 252 (6 KB)Marangiop (Talk | contribs)“Comparison of four different ribosome binding sites BBa_B0030, BBa_B0032, BBa_B0034 (Registry of Standard Biological Parts), and RBS* in Escherichia coliDH5α (white bars) and Synechocystis PCC 6803 (black bars). The translational efficiencies were...
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