The phrase "assay complete" is correct and usable in written English.
It can be used in contexts related to laboratory testing or analysis, indicating that a specific assay or test has been finished.
Example: "The results will be available shortly, as the assay complete notification has just been received from the lab."
Alternatives: "test finished" or "analysis done".
The next day, prior to the assay, complete DMEM was replaced with an XF Assay Medium Modified DMEM (Seahorse Bioscience) (1 g/ml glucose, pH 7.4) and cells were incubated at 37 °C for 1 h without CO2.
Lysyl oxidase inhibitors β-aminoproprionitrile (BAPN) or bathocuproine disulphate (BCS) phenocopied the effects of HIF-1 inactivation, and attenuated hypoxia-enhanced migration in a scratch wound closure assay; complete closure was observed by 24 hours in hypoxic cells, whereas pre-treatment with either BAPN or BCS inhibited migration with the scratch not closing for at least 30 hours.
Following the room temperature incubation, ELISA wells were washed followed by the addition of goat anti-rabbit Ig-alkaline phosphatase (Southern Biotech, Birmingham, AL) and the assay completed as per our normal ELISA protocol.
Gp120-coated cells incubated with A32 or 17b Fab fragments were washed once prior to addition of the competitor antibody and the assay completed as described above.
A stably transfected human neuroblastoma line that expresses pathogenic forms of Aβ (MC65) provides a rapid in vitro assay for the neurotoxic effects of intracellular Aβ accumulation (a 'high-throughput' assay; completed in 24 72 hours).
Cells were treated with 5 nM TFIIS siRNA #2, or 5 nM S-siRNA in 6-well plates, incubated at 72°C for 72 hours, and the assay completed as recommended by the manufacturer.
Further analysis of these mouse strains via organ culture assays, complete blood cell analysis, flow cytometry and colony forming cell assays implied that perinatal lethality in the collagen X Tg and KO mice results from lymphopenia coupled to opportunistic infections.
Further, colony forming cell assays, complete blood count analysis, serum antibody ELISA, and organ outgrowth studies established altered lymphopoiesis in all collagen X Tg and KO mice and implicated opportunistic infection as a contributor to the severe disease phenotype.
These data together substantiate that methylation of lysine 37 does not appear to play a major role in transcription, as mutation of this histone residue results in no overt phenotype in all transcription-based assays completed to date.
Now with the misincorporation assays completed with the three other polymerases, we were able to compare their enzyme fidelity by comparing the extent of the primer extension beyond the first stop site (see "*" in Fig. 2).
Among assays completed with the new limit, C-peptide was measurable in 88% of the basal samples, 87 95% of stimulated MMTT samples, and 92 94% of stimulated GST samples.
