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The competitive assay is sensitive and selective to Aβ peptides.
This immunosensor was employed in a competitive assay involving progesterone labelled with alkaline phosphatase.
The specificity of the antibody was determined by carrying out the competitive assay using various competitors.
Peptides were assayed for binding affinity using a filtration-based competitive assay to sstr2.
The possibility of using these particles as agents for DNA sensing was demonstrated in a competitive assay.
According to immunochemistry theory, a common and apt protocol for SMCs is the competitive assay.
The RVG-mediated target-specific cellular uptake of polymeric vector was established conclusively by competitive assay.
It was applied to imipramine and chlorprothixene competitive assay by the mono- 6-deoxy-6-mercapto -β-cyclodextrin self-assemono- 6-deoxy-6-mercapto -β-cyclodextrin
Besides the adapted dot blot format, a competitive assay in which the target is in solution is reported as well.
In the studied competitive assay conditions, all tested caspases except caspase 2 exhibit activity toward more than one substrate.
The specificity of the antibody was determined by carrying out the competitive assay using dexamethasone that is administered in combined therapy with LND [38], as a competitor.
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