resonance energy

resonance energy

[′rez·ən·əns ‚en·ər·jē]
(physics)
The characteistic energy at which, or very close to which, the amplitude of a resonance phenomenon is greatly enhanced.
References in periodicals archive ?
we will create stable, High-quality nc-films, Enabling the formation of multilayers for exciton funnelling by means of frster resonance energy transfer (fret).
NanoBRET TE uses bioluminescence resonance energy transfer and allows measurement of drug binding to protein targets in real time inside live cells using a simplified experimental protocol.
The T-cell receptor excision circle (TREC) assay is a dried blood spot (DBS) assay employing polymerase chain reaction (PCR)-based nucleic acid amplification and time-resolved fluorescence resonance energy transfer (TR-FRET) technology.
Chemistry professor Alexis Vallee-Belisle and his coworkers have been manipulating strands of DNA that respond directly to changes in temperature, so that they change shape and generate a fluorescent resonance energy transfer that is detectable as a light signal.
The authors used a special set of fluorescence probes to measure the transfer of the emission energy of one fluorophore to the fluorophore of its related pair in a technique called the Forster resonance energy transfer (FRET).
The great advancement of fluorescence reagents has promoted a host of more complex fluorescence technologies such as fluorescence resonance energy transfer (FRET), time-resolved fluorescence (TRF), fluorescence polarization (FP), fluorescence recovery after photobleaching (FRAP), fluorescence activated cell sorting (FACS), and fluorescence correlation spectroscopy (FCS) etc.
They describe the discovery of small molecule EPAC (exchange proteins directly activated by cAMP)-specific modulators by high-throughput screening; cyclic nucleotide analogs as pharmacological tools for studying signaling pathways; high-throughput FRET (fluorescence resonance energy transfer) assays for fast time-dependent detection of cyclic AMP in pancreatic beta cells; assessing cyclic nucleotide recognition in cells; and monitoring cyclic nucleotides using genetically encoded fluorescent reporters.
Regarding technologies, the market is segmented into fluorescence resonance energy transfer (FRET), fluorescence in situ hybridization (FISH), high-content analysis (HCA), fluorescence recovery after photobleaching (FRAP), ratiometric imaging, total internal reflection fluorescence microscopy (TRIF), multiphoton excitation microscopy (MPE), and other technologies.
We then have explored the Forster resonance energy transfer (FRET) rates between QDs of different sizes, different surface passivation, and at different distances.
In this research, the mechanism of fluorescent resonance energy transfer (FRET) from drug to nanoparticle (quantum dot) has resulted in the creation of a highly sensitive method to study interaction between drug and DNA.
FRET - Forster Resonance Energy Transfer: From Theory to Applications
The type of descriptors involved in the equation 1 are total dipole of the molecule (td) (electronic descriptor), total molecular 2-center resonance energy divided by the no of atoms (tm) (quantum chemical descriptor) and min e-n attraction for H atom(me) (electronic descriptor) (Table 3).

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