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For 10 mL of water sample, the optimized USAEME procedure used 200 μL of chloroform as extraction solvent, 15 min of extraction without ionic strength adjustment at 25 °C and 5 min of centrifugation at 4000 rpm.
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Compared with the measured current voltage (I V) curves of fabricated CMOS samples, the optimized I V results are within 3% of accuracy.
Finally, using a set of 3 samples, the optimized model was successfully transferred to a secondary instrument located in a quality control (QC) laboratory.
In order to confirm the presence of PXD in the subject samples, the optimized experimental conditions of two reported HPLC methods (Siebers et al. 2014; Shehzad and Shah 2013) were employed.
Using a set of external validation samples, the optimized calibration models for PC, C1, C2 and C3 exhibited bias values of −1.07%, 0.28%, −1.21% and −1.00%, and RMSEP of 2.43%, 1.44%, 1.51%, and 2.05%, respectively.
The SEM photographs of the surface morphology with various ohmic contact systems after annealing at 850°C for 30 s: (a) sample 1, Ti/Al/Ti/Au; (b) sample 2, Ti/Al/Ni/Au; (c) sample 3, Ti/Al/Ta/Au; and (d) sample 4, the optimized Ti/Al/Ta/Au.
The sample with the optimized thickness, TP (3L), was chosen to be attached to the STNA and LTNA scattering layers, with a thickness of around 1.8 μm as shown in Figure 1c,d.
The Cit3−/M molar ratio R is 1.0 in each case, and the pH values are a 5, b 7, and c 9. Time-course phase and morphology evolution was studied for the 0.2ZGC sample under the optimized conditions of 180 °C, pH = 5, and Cit3−/M molar ratio R of 1.0.
The cell line was established from the primary culture of breast cancer biopsy sample using the optimized feeder layer technique [ 15, 16].
The experimental results showed that the samples of the optimized design had better corrosion resistance than those of the conventional design.
In order to characterize the hydrolysates based on their molecular weights, Tris glycine sodium dodecyl sulphate polyacrylamide gel electrophoresis (Tris Glycine SDS-PAGE) was performed on samples from the optimized enzymatic hydrolysis.
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