Piljic, A. & Schultz, C. Simultaneous recording of multiple cellular events by FRET.
Jares-Erijman, E. A. & Jovin, T. M. Imaging molecular interactions in living cells by FRET microscopy.
(c) Relationship between N and the distance d as determined by FRET.
Mitochondrial ATP content was determined by FRET image analysis of cells transfected with pcDNA-ATeam1.0338.
The ligand quadruplex interactions were further evaluated by FRET, ITC, and PCR stop assay.
Seong, J. et al. Visualization of Src activity at different compartments of the plasma membrane by FRET imaging.
We used the DOnly models to fit the corresponding DA sample under the assumption that all donor states are quenched equally by FRET.
By FRET microscopy, we have visualized crucial molecular binding events during cell differentiation, signaling flow, growth and/or death13,14,15,16,17,18.
For latex films cast from these two-component particles, we studied the diffusion rate of the high molecular weight polymer by FRET.
By FRET analysis, a strong driver signal at the phase I is shown and then proceeds to cell death at the phase II.
To gain further insight into the relationship between CaM binding and tetramerization of the wt ABCD domain, the interchange between tetrameric assemblies was monitored by FRET.
