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This assay uses a chimera of split forms of renilla luciferase (RL) and green fluorescent protein (GFP).
This assay uses a common forward primer based on the 5.8S region and two reverse primers, which is specific for the two categories.
However, this assay uses a fluorogenic peptide containing 7-amino-4-methylcoumarin (AMC), which becomes the cause of false positive hits from screenings.
This assay uses caffeine for G2-checkpoint abrogation and it was applied to obtain an internal control for radiosensitivity testing, which simulates conditions similar to those of the highly radiosensitive lymphocytes of AT patients.
This assay uses human CYP1A2 to measure the demethylation of luciferin 6' methyl ether (Luciferin-ME; Promega-Glo) to luciferin.
This assay uses recombinant DFS70 (expressed in E. coli) coated onto paramagnetic beads and is designed for the BIO-FLASH instrument.
This assay uses the red pigmentation of yeast ade2 mutants to score chromosome loss.
This assay uses the double-stranded DNA-specific dye PicoGreen to measure a change in fluorescence after DNase I digestion enabling a determination of activity.
This assay uses a monoclonal antibody to capture free MMP-1 and assesses its levels by measuring the amount of cleaved collagen peptide by monitoring fluorescence.
This assay uses an artificial school of model fish to evaluate the schooling tendency of an individual using a standardized and repeatable stimulus.
This assay uses acyl-CoA as the thioester substrate, with colorimetric detection of TNB2− formed when DTNB reacts with the hydrolyzed product HS-CoA[28].
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