Sentence examples for equivalent assay from inspiring English sources

Most notably, the time required to perform an assay to an equivalent assay mass variance is greatly reduced with a fast-neutron system, by more than an order of magnitude compared with that of the thermal-neutron system, due to the reduced probability of random summing with the fast system.

Therefore, we generated an equivalent assay system for scoring MRF in tetraploids with only bivalent formation.

However, we were unable to establish an equivalent assay for H2B de-ubiquitination because of the relatively low levels of H2Bub in mammalian cells (West and Bonner, 1980).

All the inhibition assays were conducted using membrane-bound F1Fo for both membrane preparations and the purified F1 preparation, provide equivalent assay results, and are highly convenient and less time-consuming.

The 77 167 fragment of R133C, which corresponds to the MBD alone, lost the ability to form a stable complex with methylated DNA, whereas 1 205[R133C] was essentially WT by an equivalent assay (Fig.  5A and B).

Unfortunately, the commercial radioimmunoassay for cAMP was withdrawn from the market while the study was already advanced and it was not possible to find an equivalent assay for tests at higher peptide concentrations to ensure saturation was achieved for all peptides.

To determine differentiation capacity, cNSC lines were taken at P4 and compared to primary fetal cerebral lines grown in equivalent assays.

We determined IGF-IR/IR signalling pathway endpoints in dose- and time-varying experiments, and performed mitogenic dose response equivalent assays to derive EC50 values, and correlated these with IGF-IR/IR ratios.

These cells presumably express OCT4, as OCT4 is present in all ICM cells in equivalent assays, but they could not be assigned to either the epiblast or PrE lineage.

We originally developed this assay to assess activated ERK 1 and 2 levels in fixed GH3/B6/F10 cells [ 10] and subsequently adapted it to equivalent assays for p38s and JNKs, and now in this study for the phosphorylated transcription factors Elk-1 and ATF-2.

Three-dimensional cultured skin models (Testskin living skin equivalent-high; Toyobo, Tokyo, Japan) were cultured at 37°C in living skin equivalent-assay medium in a 5% CO2 humidified incubator for 48 hours to evaluate gene expression and for 7 days to analyze ceramide synthesis.