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To exclude this possibility, we carried out a 'promoter swap' experiment.
Similar results were obtained using a green fluorescent dye for MA- cells and a red dye for MP cells (dye swap experiment, data not shown).
To do this, we performed a "swap" experiment in which a proportion of SGLs were swapped with an increasing number of their DGL counterparts.
The UTR swap experiment has revealed that the direction of growth phase-dependent translational control is encoded in the 3'-UTR.
To demonstrate that RibH1 and RibH2 are LSs in vivo, we developed a plasmid swap experiment based the instability of two vectors from the same incompatibility group harbored in the same bacterial population.
To address this issue we designed a plasmid swap experiment assuming that the pribH1Km plasmid that is harbored by the ribH1-ribH2 strain is essential for the growth in TSB medium (poor in riboflavin) (Figure 2A).
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For each sample, a dye-swap experiment was realised simultaneously.
At least one dye-swap experiment per generation post-cloning was performed.
A UTR-swap experiment was performed to identify which UTR determines regulatory direction.
Each amplified sample was hybridized twice against a common reference pool in a dye-swap experiment.
Four hybridizations, including the dye-swap experiment, were carried out between the target and the reference samples.
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