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Improved differentiation between luminescence decay components by use of time-resolved optical activity measurements and selective lifetime modulation.

The analysis of luminescence decay experiments from proteins is typically modeled as a combination of independent first-order decay functions. However, Poisson noise in the photon counting experiment limits the ability of this approach to resolve decay components from separate lumiphores with simila...

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Dettagli Bibliografici
Autori principali: Schauerte, J A, Gafni, A, Steel, D G
Natura: Artigo
Lingua:Inglês
Pubblicazione: 1996
Soggetti:
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC1225168/
https://ncbi.nlm.nih.gov/pubmed/8785358
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