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Receiver-operating characteristic curves were calculated by plotting sensitivity versus (1 -specificity), allowing calculation of area under the curve (AUC).
The IC50 values of various formulations were calculated by plotting a graph of percent cell viability vs. concentrations.
Specific growth rates were calculated by plotting the natural logarithm of biomass over time in its exponential phase.
The rate constant values analogous to different concentrations of gabapentin were calculated by plotting the slopes of log A /A??At versus time under pseudo-first order conditions (Table?2).
Dissociation constants were calculated by plotting bound MMP2 aptamer versus protein concentration using the following equation: Y = BmaxX/ Kd + X), where Bmax is the extrapolated maximal amount of bound aptamer/protein complex.
The method of least squares was used, and the coefficients (a) and (b) were calculated by plotting log Y against log X according to Hile (1936); Bagenal and Tesch (1978), and Le Cren (1951) where log Y = log a ± b log X.
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The Urbach energy is calculated by plotting lnα vs. E.
Sample concentration providing 50% inhibition (IC50) was calculated by plotting the inhibition percentage against sample concentration.
In practice, the band-gap is calculated by plotting hν versus (αhν 2.
Value k can be calculated by plotting the first order rate equation for a batch cell [Eq. (2)] versus t.
The IC50 value of each compound was calculated by plotting the inhibition percentage against concentration of the tested compounds and the results were expressed in μM.
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