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Viral RNA was extracted from 140 μL each serum sample using the QIAamp Viral RNA Mini Kit (Qiagen, Germany) according to the manufacturer's instructions.
Cell-free genomic DNA was isolated from 400 μl of the serum sample using the QIAamp blood mini kit (Qiagen, Hilden, Germany).
However Remel brand was the most accurate brand using the cut-off values of 1/160 and 1/320 (87.91% and 70.23% respectively) Tables 6, 7, 8 show the distribution of the results of 91 serum sample using the 4 Widal brands at a 1/80, 1/160 and 1/320 cut-off values for anti-H antibodies in relation to their corresponding IgM anti-LPS ELISA results.
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In addition, the modified electrode was successfully applied for the determination of analytes in urine and serum samples using the standard adding method with satisfactory results.
Thus, the modified electrodes were successfully applied for the determination of DA, UA and Trp in urine and serum samples using the standard adding method with satisfactory results.
The results showed that the analytical performance of the determination of the 20 amino acids in tea, urine and serum samples using the home-made golf ball-assisted ESI source is better than that of a commercial ESI source.
The operating characteristic of the integrated bioreactor/detector unit has been utilized in the determination of glucose in serum samples using the electroactive polymer as mediator in the re-oxidation of GOx and amperometric monitoring.
Dengue virus RNA was extracted from serum samples using the QIAampR Viral RNA mini kit (Qiagen).
Figure 2A shows the merged gel filtration HPLC chromatograms from 16 individual serum samples using the Superdex Peptide 10/300 column.
A one-step TaqMan® real time quantitative RT-PCR was performed in serum samples using the Light Cycler 2.0® (Roche Diagnostics).
Results in this manuscript are reported for an immunoglobulin concentration of 4 mg/mL for Day 70 serum samples using the same equation for calculation of percent inhibition.
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