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Synthesis rates of genome-wide proteins have been calculated from experiments when yeast cells grow mitotically in glucose medium [ 43].
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The means and standard deviations were calculated from experiments performed in triplicate and are presented as n-fold differences in expression.
The apparent dissociation constants were calculated from experiments carried out in triplicate.
The standard deviation was calculated from experiments conducted in triplicate and is indicated by error bars on the figures.
The most important feature was that the RNA polymerase (RNAP) and ribosome concentrations were expressed as a function of the specific growth rate, μ, which varied during batch cultivation and was calculated from experiments.
The 578 A i and 434 A i absorbance terms in eq 8 can then be written as The molar absorptivity terms 578εH2I and 434εH2I were calculated from measurements in 1 M HCl where H2I is a strongly predominant species; the molar absorptivity terms 578εI and 434εI were calculated from experiments at pH 12 where I2– strongly predominates.
However it cannot explain the difference observed with what had been calculated from AFM experiments with amylin peptides (1.1 nm/min) [34] or with Aß1 40 protofibrils (1.3 nm/min) [35].
Standard deviations are calculated from triplicate experiments.
Closed symbol; Y-94, Open symbol; YKX1 Standard deviations are calculated from triplicate experiments.
The volumetric mass trasnfer coefficient a1k1 and Henry's constant can be calculated from these experiments.
These fluxes normalized by maximum flux magnitudes in Figure 3 are calculated from the experiments for cases (a) A02, (b) A10, and (c) A20.
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