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. 2010 Dec 15;124(2):181–185. doi: 10.1242/jcs.077313

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Fig. 2. — Effects of rrm3Δ on Sml1 levels and bulk genome duplication in mec1-4ts. (A) MYC–Sml1 levels in the indicated strains following an α-factor arrest and release. The signal corresponding to the MYC–Sml1 is quantified and normalized to that of the tubulin band. Normalized signals are then expressed relative to the t=0 sample, which was set to 1 for each strain. ‘UnT’, untagged control strain. (B) FACS profiles of the samples in A. (C) Status of ChrIII in the indicated strains. Two independently derived rrm3Δ mec1-4ts tel1Δ strains were analyzed.