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Eight-point dose response curves were generated for 24 anticancer drugs using an automated compound-screening platform [13].
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Using an automated cell-based screening assay, Balgi et al. [14] identified that niclosamide can rapidly increase autophagosome formation.
A well-established approach for this is high-throughput screening (HTS), which includes screening a large number of chemical compounds against a target using an automated bioassay [1].
Radiosynthesis of [68Ga]3 was performed using an automated synthesis module by heating 20 μg of compound 3 with [68Ga]GaCl3 aq).
A fluorescence image of each well was captured by using an automated imaging system at 16 and 28 h post-incubation with the test compounds (Fig. 1D).
Sorof et. al. [ 11], using an automated oscillometric monitor, did show a prevalence of HBP ≥ 95th percentile) at 19% in school children at the first screening.
Images were analyzed using an automated computer algorithm Quimp3.
Water and sucrose consumption were measured using an automated lickometer.
For mutation screening, exon 20 of the BRCA2 gene was amplified and PCR products were directly sequenced using an automated fluorescence-cycle sequencer.
For the screening of PCR-based markers over the whole population, leaf tissue samples were collected from all individuals and DNA extracted using an automated extraction protocol.
This work used an automated robotic clone picking system to establish over 250 insect clones of a Helicoverpa zea cell population to be screened for virus production.
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