Sentence examples for this assay is designed from inspiring English sources

This assay is designed to find new PrP‐res inhibitors, which may make good candidates for in vivo anti‐scrapie testing.

This assay is designed for broad applicability and accessibility, employs modifications of commercially available components, and allows more than 25 independently selected gene-specific primers to be used simultaneously.

This assay is designed to recapitulate the events that occur when quiescent vasculature encounters collagen I outside the vascular basement membrane during a wound healing process.

This assay is designed to determine both phosphorylation and dephosphorylation of tau by assessing the incorporation of radioactively labelled phosphate residues into the tau protein.

This assay is designed to detect the biologically active natural and recombinant human TGF-β1.

This assay is designed to generate amplified and biotinylated sense-strand DNA targets from the entire expressed genome without bias.

This assay was designed to target the 16S rRNA gene with a DNA/RNA chimeric primer.

While this assay was designed for use in Ae. albopictus, it will have broader application in other anthropophilic mosquitoes.

The primers and probes employed in this assay were designed from conserved regions within toxin biosynthesis genes from most of the representative cyanobacterial genera.

Although this assay was designed for the selection of catalysts active in DNA hydrolysis, it can be adapted to detect most types of substrate cleavage reaction.

This assay was designed to assess the cross-linking activity of TG-2 between two proteins.