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The sensitivity and specificity of each assay were evaluated using serial dilutions of cell line DNA containing the relevant mutations in a wild-type background.
Differences in mean values of absorbance on WST-1 assay and number of colonies in the colony-forming assay were evaluated using the Student's t-test for unpaired data.
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The assay was evaluated using online analysis, identified influenza viruses and clinical samples.
The specificity of the minisequencing assay was evaluated using 35 strains of L. plantarum group species.
The specificity of the minisequencing assay was evaluated using 63 strains of L. casei group species.
This multiplex one-step RT-PCR assay was evaluated using 376 samples collected during the year 2003.
The assay was evaluated using clinical samples and the results indicated the suitability and simplicity of the test as a rapid, field diagnostic tool for VHS virus.
The efficiency of this assay was evaluated using recombinant HLA-DP0401 molecules (HLA-DP) produced in insect cells and 13 peptides from human telomerase reverse transcriptase (hTERT).
The specificity of the real-time PCR assay was evaluated using several DNA viruses including goatpox virus (Accession number: AY077836.1), sheeppox virus (Accession number: AY077833.1), and swine pseudorabies virus (HB-98 vaccine Strain).
In this study in 2011, the assay was evaluated using 6 proteins, 3 already reported cancer biomarkers, as well as 3 cytokines (CEA, HER2, ENG and TNF-a, IL-8, MIP/CCL4 respectively) [108].
The performance of the assay was evaluated using a pilot excretion study that involved six subjects receiving C.E.R.A. Validation data demonstrated an excellent reproducibility and ensured the applicability of the assay for anti-doping purposes.
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