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The specificity, sensitivity, and robustness of the assay were evaluated for common mutations in the FV, PII, MTHFR, and FGFR3 genes.
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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.
A reverse transcription Linear-After-The-Exponential polymerase chain reaction (RT LATE-PCR) assay was evaluated for detection of foot-and-mouth disease virus (FMDV).
In addition, the assay was evaluated for clinical serum specimens, and received a good correlation with those obtained by the referenced electrochemiluminescent (ECL).
The assay was evaluated for inter-day and intra-day precision based on %CV < 25 with target acceptance of PC end point log10 titers from each set of PC (intra-run) and all accepted runs (inter-run).
After successful amplification of desired DNA fragments by this primer pair, the PCR assay was evaluated for their efficiency to amplify DNA extracted from cooked and autoclaved meat and meat emulsion.
The assay was evaluated for inter-day and intra-day precision based on coefficient of variation (%CV) with target acceptance of PC endpoint titers (log10) from each set of PC (intra-run), and all runs (inter-run) are less than 25.0%.
The pentaplex PCR assay was evaluated for analytical specificity and sensitivity.
The reproducibility of the real time assay was evaluated for initial DNA content, presence of PCR inhibitors etc.
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