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Amplified luminescent proximity

Amplified Luminescence Proximity Homogeneous Assay (AlphaS-creen ) technology have been reported [50,51]. With an HTS methodology in hand and orthogonal assays previously developed [47-49], nonpeptide antagonists of methyl lysine binding should appear from diversity screening approaches in the near future. [Pg.337]

AlphaScreen (amplified luminescent proximity homogeneous assay) PerkinElmer Life Sciences Donor beads produce singlet oxygen that induces fluorescence in proximal acceptor beads bead-bead proximity results from engagement of binding partners immobilized on the two bead types... [Pg.88]

In order to avoid the described problems, antibody-based assays have been developed. As mentioned above, usually a primary antibody recognizes the modification, which in turn is then quantitated. One of these approaches is based on the technology of AlphaScreen (Amplified luminescent Proximity Homogeneous Assay) [51, 52], also known as luminescent oxygen channeling immunoassay (LOCI) [53], a method that can be used to study protein-protein interactions in general. In this case the enzymatic transfer of acetyl groups to a histone peptide is determined. [Pg.108]

Amplified Luminescent Proximity Homogeneous Assay (AlphaScreen )... [Pg.238]

The Amplified Luminescent Proximity Homogeneous Assay (AlphaScreen ) developed by BioSignal, is a bead-based, non-radioactive assay technology. It uses the principle of luminescent oxygen channeling, which was first described in 1994 by Ullman [173], who two years later demonstrated a broad spectrum of applications for such immunoassays [174]. This principle senses the proximity of two beads, a donor and an acceptor bead, which is mediated by the interaction of molecules on the surfaces of the two beads. [Pg.644]

AlphaScreen Amplified luminescence proximity homogeneous assay... [Pg.455]

Parameters Radiometric proximity assays (SPA, Flashplate) Fluorescence polarization (FP) Time- resolved fluorescence (HTRF) Amplified luminescence (ALPHAScreen) Enzyme (p-galactosidase) complementation Electrochemilumines cence... [Pg.378]

Because of their narrow emission bands, long luminescence lifetimes, and absorption profiles that span from the near-UV to the near-IR, lanthanides have been investigated for applications such as light-emitting diodes [36] and optical amplifiers [37]. However, the tendency of lanthanides to aggregate leads to self-quenching, which limits their luminescence efficiency and lifetimes. Also, proximity to solvent molecules which can act as quenchers limits their potential use as optoelectronic materials [38,39]. [Pg.98]


See other pages where Amplified luminescent proximity is mentioned: [Pg.39]    [Pg.423]    [Pg.10]    [Pg.159]    [Pg.167]    [Pg.226]    [Pg.228]    [Pg.424]    [Pg.190]    [Pg.39]    [Pg.423]    [Pg.10]    [Pg.159]    [Pg.167]    [Pg.226]    [Pg.228]    [Pg.424]    [Pg.190]    [Pg.97]    [Pg.291]    [Pg.311]   


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