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The fluorescence decay was fitted well by a single exponential, yielding a fluorescence lifetime of 2.6±0.1 ns.
We bleached the entire equatorial ring in cells of control embryos, or the entire shifting ring in cells of embryos treated with blebbistatin for at least 30 min. For control embryos, the recovery curve was well fitted by a single exponential, yielding a characteristic turnover rate of 90 s ± 3 s.
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The profile was best fit by two exponentials, yielding t1/2 values of 9.9 and 83.5 s for the unfolded state (U) → intermediate state (I) (transition 1) and intermediate (I) → native state (N) (transition 2), respectively (Table 6).
The graph was fitted with an exponential function, yielding a familiarization time constant τfam = 4.6 laps (r2 = 0.916).
Data were fitted using a double exponential function, yielding fast (B ) and slow (C ) recovery.
Plot of 1-CDF was best fit to a single exponential curve, yielding τ1 = 33 ± 2 s (n = 87 complexes).
In each case, the data fit well to a single exponential function yielding a rate constant of about 1 min–1.
In order to facilitate interpretation, the resulting regression coefficients for categorical variables were back-transformed to their exponential (exp, yielding the ratio of the GM of FeNO of each exposure category vs the reference category.
Under the monomer condition, unwinding curves for RD31 can be fit to a single exponential function, yielding the unwinding times tunwind = 6.3 ± 0.9 and 1.6 ± 0.2 min at 20 μM and 1 mM ATP, respectively.
Data were fit with a single-exponential function, yielding a recovery time constant of 16 s (Fig. 4D).
Rates were first measured in the absence of added GTP (as in Figure 4) where the intrinsic rate of pyrophosphate removal for each substrate was readily measurable; time courses fit well to a single-exponential equation, yielding kobs values for both substrates that were almost identical to that observed for the G 1 A73-tRNA (Table 2).
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