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The applicability of the assay with field samples was demonstrated using net concentrated seawater samples, un-spiked or spiked with known amounts of cultured cells.
Assay applicability to complex samples was demonstrated using mixtures containing RNA sequences from two related, harmful algal bloom-causing Alexandrium species.
A statistically significant difference in the pattern of fungi that were present in the respective samples was demonstrated using the Phylogenetic (P) test (P < 0.0001).
The differences based on the percent of total DNA reads of in the pooled samples from asthma patients and non-atopic controls are shown in Tables 1 and 2. A statistically significant difference in the pattern of fungi that were present in the respective samples was demonstrated using the Phylogenetic (P) test (P <0.0001).
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The potential of polarization-modulation infrared reflection-absorption spectroscopy (PM-IRRAS) for in situ and time-resolved studies using powder samples is demonstrated using as an example the NOx storage-reduction behaviour of a Pt-Ba/Al2O3 powder catalyst.
In 9 samples toxin was demonstrated using immunoassay, while C. difficile was not cultured.
Simultaneous detection of horseradish peroxidase (HRP) utilizing a 5 μL sample analytical volume was demonstrated using a single μPAD.
A method to extract thin foil samples of substrate/coating interfaces was demonstrated using a focused ion beam approach.
Process improvement in microarray assay performance was demonstrated using samples prepared from commercially available materials and two metrics - diagnostic performance and the reliable range of measurement.
The effect of a rotating process on cell capture was investigated, and the capture efficiency was demonstrated using blood samples from healthy donors spiked with human non-small cell lung cancer NCI-H16500) and breast cancer (MCF-7) cells.
The applicability of the elaborated method was demonstrated using human urine samples.
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