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Ct values from both assays were comparable (data not shown).
Intra-assay and inter-assay coefficients of variation of both assays were comparable to the OPPV qPCR assay reported by Herrmann-Hoesing et al. (2007).
Similar(58)
The compared gene assays were comparable in efficiency and over 96% for cDNA from samples and controls.
Overall, the sensitivity of the DML and Slidex assays were comparable in both sub-studies.
The results showed that for compounds that were predominately metabolized by CYP mediated mechanisms, the intrinsic clearance values from the two assays were comparable.
The velocities observed in TIRF assays were comparable to those in multi-motor gliding assays where the motor was attached to the coverslip surface, and microtubules slid over the surface (Table 1).
The operational characteristics of the molecular assays were comparable.
These results indicated that most of the assays were comparable to TP-PA when the serum samples were tested undiluted.
Laboratory A showed high variability between replicates using detection of the 3-day MN titers by CPE (91.7%), as the data from two replicate assays were comparable whereas the data from the third assay were inconsistent (data not shown).
Efficiencies for all assays were comparable as determined from standard curves generated from amplifications of serial dilutions of a human cDNA pool (average efficiencies were 0.95 and 0.96 for the assays of HERV-W elements and adjacent genes, respectively).
The imprecisions of the Simple Plex assays were comparable to those of the traditional ELISAs, which were evaluated using replicates of the same serum sample pool, to be 9.0, 6.6, 14.5, and 8.3 %, for IL-1β, TNF-α, IL-6, and IL-10, respectively.
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CEO of Professional Science Editing for Scientists @ prosciediting.com