We have also gone on to demonstrate the more general applicability of our assay by using it to quantify other genetic events.
We have developed a feline IFN-γ ELISPOT assay and used it to determine FIV-specific T-cell epitopes recognized by infected cats.
Second, we developed a large-scale and non-invasive optogenetic assay and used it to activate Hcrt neurons in freely behaving larvae.
In order to further investigate the role of PfCDPK1, we established a high-throughput in vitro biochemical assay and used it to screen a library of over 35,000 small molecules.
To validate this two-color flow cytometric assay, we used it to determine the invasion phenotypes of three laboratory strains of P. falciparum, 3D7, Dd2, and HB3, which have all had invasion profiles generated previously by multiple laboratories.
In the Genomic Assay® we used it to promote and signal the formation of heteropolymeric, specific triplex useful in diagnostics and analysis.
Second, because WNVKUN is a convenient strain for cell-based assays, we used it to correlate the observations we made regarding Xrn1 resistance in vitro with the formation of sfRNAs during infection.
As laser scanning confocal microscopy allows direct visualization of molecule localization in cells, it was used to assay MPO binding to platelets.
It is still used, however, to assay gold and provides a reasonably accurate guide to quality.
If the array is integrated into a chromosomal region near the centromere, it can be used to assay cohesion between sister chromatids the linkage between sisters resists chromosome separation (and that of the arrays) until the onset of anaphase, so a single focus is observed in metaphase-arrested cells if cohesion is maintained (Straight et al. 1996).
