Multiphoton time-domain fluorescence lifetime imaging microscopy: practical application to protein-protein interactions using global analysis
Förster resonance energy transfer (FRET) detected via fluorescence lifetime imaging microscopy (FLIM) and global analysis provide a way in which protein-protein interactions may be spatially localized and quantified within biological cells. The FRET efficiency and proportion of interacting molecules...
المؤلفون الرئيسيون: | Barber, P, Ameer-Beg, S, Gilbey, J, Carlin, L, Keppler, M, Ng, T, Vojnovic, B |
---|---|
التنسيق: | Journal article |
اللغة: | English |
منشور في: |
2009
|
مواد مشابهة
-
Deep-tissue multi-photon fluorescence lifetime microscopy for intravital imaging of protein-protein interactions
حسب: Fruhwirth, G, وآخرون
منشور في: (2009) -
Monitoring conformational changes of proteins in cells by fluorescence lifetime imaging microscopy.
حسب: Calleja, V, وآخرون
منشور في: (2003) -
Mapping femtosecond pulse front distortion and group velocity dispersion in multiphoton microscopy
حسب: Tullis, I, وآخرون
منشور في: (2006) -
Mapping femtosecond pulse front distortion and group velocity dispersion in multiphoton microscopy
حسب: Tullis, I, وآخرون
منشور في: (2006) -
Dynamic imaging of protein-protein interactions by MP-FLIM
حسب: Ameer-Beg, S, وآخرون
منشور في: (2005)