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Subsequently, topo-I and IIα-mediated relaxation and antiproliferative activity assays were evaluated for 5.
Quantitative data from cell counts, FACS analysis, western blot analysis, and other assays were evaluated for statistical significance using one-way analysis of variance (ANOVA).
At first, the 42 assays were evaluated for which both assay nucleotides had identified sets of BACs (Table 1).
Quantitative data from Western blot analysis, wound healing assay, spheroid migration assay and matrigel invasion assays were evaluated for statistical significance using one-way ANOVA.
The serotype-specific DENV RT-PCR assays were evaluated for their clinical performance by retrospectively testing 85 serum samples obtained from patients presenting with acute dengue (Table 3).
Quantitative data from cell counts, Western blot analysis, and other assays were evaluated for statistical significance using one-way analysis of variance (ANOVA).
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Until more different examples of Two-Temperature LATE-PCR assays are evaluated for inter-assay variability, however, we recommend the use of the use of reference samples of known genotypes as internal controls for every genotyping experiment.
The specificity, sensitivity, and robustness of the assay were evaluated for common mutations in the FV, PII, MTHFR, and FGFR3 genes.
This assay was evaluated for its diagnostic utility using blood samples collected from experimentally and naturally infected cattle in China.
Drug release studies carried out at two different pHs and the MTT assay was evaluated for DOX-loaded CMC/GQD nanocomposite hydrogel films against blood cancer cells (K562).
The specificity of the MB-based PCR assay was evaluated for various E. coli strains as well as bacteria species that are present in nature.
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