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The RT-LAMP method detected specifically PLDMV and was highly sensitive, with a detection limit of 1.32 × 10−6 μg of total RNA per reaction.
Our assay was highly sensitive with a limit of detection of 5.6 ng mL−1, which is comparable to those of other currently available sensitive methods such as ELISA and luminescence-based assays.
In addition, the RPA-LF assay was highly sensitive, with a detection limit as low as 20 fg of target DNA or 1.05 × 101 cfu of bacteria in pure culture, and highly specific, exhibiting no cross-reaction with Staphylococcus aureus, Escherichia coli, Listeria monocytogenes, Shigella, Enterobacter aerogenes, or Campylobacter jejuni.
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Although the diagnostic performance of EUS is difficult to evaluate, reports indicate that overall the technique is highly sensitive with sensitivities as high as 79%100%% being reported [ 44, 45].
While BFAST is highly sensitive with the use of 10 indexes, as shown here, if the sensitivity were not satisfactory for a given purpose, to the addition of additional genomic indexes would improve the sensitivity with a modest increase in the computational time.
It was found that the choice between the two machining modes is highly sensitive with respect to manufacturing sustainability.
In addition, the probe is highly sensitive (with the detection limit of 0.12 μM) and highly selective to Fe3+ over other biologically relevant metal ions.
We can thus conclude that the developed assay is highly sensitive, with improved throughput and with excellent possibility to detect multiple infections.
Dilution assays using the in vitro transcript showed that the primer/probe set is highly sensitive, with a detection limit of 1 fg/μl.
The method is proved to be highly sensitive with the linear range of 0.05 6.0 μg L−1 and the limits of detection of 0.034 and 0.011 μg L−1 for naproxen and 6-O-desmethylnaproxen, respectively.
Because this cell line proved to be highly sensitive with relatively lower cell viabilities at comparable concentrations used for reporter gene assays, the final concentrations for the majority of compounds were adjusted to prevent cytotoxicity and accommodate healthy cell viability values (>80%).
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