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Data was obtained as cell counts (mean of three separate wells) for each treatment, with experiments performed in duplicate.
This corresponds to the low range of the count rates observed in the experiments performed in this study, which for the full spectrum, were equal to about 400 kcps.
Cell counts are expressed as the mean±SEM of three independent experiments performed in triplicate.
This represents the probability of observing zero counts in one or more of the n injection experiments performed.
In spreading experiments, a minimum of fifteen cells from each treatment group was counted, with 3 replicates per experiment, and three independent experiments performed.
All experiments performed in quintuplicate; cells counted on a hemocytometer.
designed the experiments; R.U. performed most of experiments; C.A. performed Ailsa Craig genome editing; K.O.
Table of total peptide counts (raw spectral counts) for each mass spectrometry experiment performed on mSWI/SNF complexes purified using HA-tagged baits.
Two series of experiments were performed.
Different sets of experiments were performed.
Over 3400 computational experiments and counting of octamers were performed within the integrated knowledge/programming environment of the CyanoBIKE instance of BioBIKE [ 26].
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