Exact(50)
Each analytical run was prepared and assayed within a 28-h period.
In determining the intra-day accuracy and precision, four quality control (QC) samples (n = 6) were assayed within the same day.
The effect of pH on activity of 0.1 U of purified enzyme was assayed within a pH range of 1 10 using 40 mM n-propanol as a substrate and 50 mM of the following buffers: HCl KCl buffer (pH 1), tartaric acid (pH 2), citrate buffer (pH 3), acetate buffer (pH 4 5), phosphate buffer (pH 6 8), tris HCl buffer (pH 9) and carbonate bicarbonate buffer (pH 10).
Treated DNA specimens were stored at −20°C and were assayed within two weeks.
Embryos and larvae produced by the transgenic fish are readily arrayed, drugged and assayed within microtiter plates, making them suitable for high throughput screens.
Finally, in a few of the candidates, few SNPs were assayed within or close to the gene, although these were generally selected as having significantly different alleles between the populations – these are HCN2, and the primary candidate PTH.
Similar(10)
Technical consistency of assays within and across cohorts was also tested using three random samples.
Additionally, the four antioxidant activity assays within the same extraction medium revealed the following order: ORAC > HORAC > DRSC > FRAP.
Reproducibility of the miRNA assays within and across studies supports that these assays are specific for mature miRNAs, as also claimed by the manufacturer.
Vesicles were used in assays within 15 min of being made.
We conducted a series of targeted reciprocal mating assays within and between isolates.
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