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Under optimized conditions, the method demonstrated linear calibration curve with good detection limit (0.028 ng mL−1) and R2 = 0.9983.
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The method demonstrated a good linear range between 1.25 and 10 ng/ml.
This proposed method demonstrated a good linear correlation coefficient of 0.9937 and a detection limit (3 σ/K) of 0.018 μg mL−1 for hsDNA.
Taking the CdTe@[emim]MP-amimRG nanocomposite as the electrochemical sensor of puerarin, the proposed method demonstrates the linear range over 0.01 4.0 μmol L−1 with the detection limits of 6 nmol L−1 in the aqueous solution (S/N = 3).
The results derived by using the ATP and DNA methods demonstrated a significant linear relationship (r = 0.95) and IC50 values obtained from the ATP and DNA assays were similar: 55 µM of EGCG for LNCaP and 35 µM EGCG for MCF-7 cells at 72 h.
High correlation coefficient, R, demonstrates linear relationship.
The analysis of the impedance spectra performed by the distribution of relaxation times and non-linear least square methods demonstrated that the electrode process is limited by several rate-determining steps.
The accuracy and efficiency of the method is demonstrated using linear and nonlinear examples relevant to geophysical flows.
Support vector machines (SVMs) [ 65, 66] were used by many participating teams, with non-linear kernel-based methods demonstrating clear advantages over linear SVMs.
The proposed method was demonstrated to be linear, accurate, precise, robust and specific, based on method validation.
The method is demonstrated on a linear Fresnel reflector array and a number of variable iteration examples presented.
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