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However, for the ECL peaks at 2.30 V, the current densities and light intensities linearly increased with increasing AA concentration, suggesting that the reducing radical was formed through the direct oxidation at the electrode surface.
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We show that the ratiometric emission intensity linearly decreases with the propanol exposure and that the ratiometric intensity is widely independent of the total liposome concentration.
The signal intensity linearly correlated with Hg2+ concentration ranging from 2.80 to 88.9 nM with a detection limit of 0.885 nM.
Its peak fluorescence intensity linearly increases with the increase the concentration of His in the range of 2.8 5 × 10−3 M with the detection limit of 2.2 × 10−3 M.
The DP of TDC_B (rainfall intensity linearly increased with time) was the lowest, while that of TDC_E (rainfall intensity kept constant with time) was the greatest.
In 0.1 M phosphate buffer solution at pH ∼ 7.0, the differential pulse voltammetric peak intensity linearly correlates with DA concentration in two regions, viz.
Upon irradiation with UV light, a band at ∼560 nm appeared, due to the conversion of spiropyran to zwitterionic merocyanine, its intensity linearly increasing with DSSP too.
Under optimal conditions, the CL intensity linearly increased with the concentration of the trigger DNA from 0.5 × 10−6 to 1.0 × 10−11 M and the detection limit is 7.0 × 10−12 M.
Its peak fluorescence intensity linearly decreases with the increase the concentration of His in the range of 1.6 × 10−6 2 × 10−4 M with the detection limit of 5.2 × 10−7 M.
The fluorescence intensity linearly decreases with the increase of H2O2 concentration in the range from 2 × 10 − 9 to 2 × 10 − 4 M with the detection limit of 6.8 × 10 − 10 M.
In the time limit where fluctuations are already averaged out, the time integrated measured intensity linearly increases with the integration time, indicating steady state behavior (Fig. 5(a)).
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