Paper
28 February 2014 Enhancing stimulated emission-based fluorescence detection with interferometric setup
Shen-Shou Max Chung, Jia-Hui Deng, Po-Lin Lin, Fu-Jen Kao
Author Affiliations +
Abstract
Fluorescence lifetime imaging microscopy (FLIM) can reveal important biological information and recently stimulated emission (SE) has been applied in FLIM to improve the spatial resolution of micrographs and detect fluorophore over a long working distance. An issue with SE is that the SE signal is much weaker than the probe laser beam that is used to generate the SE, therefore the signal to background ratio is low. Here we demonstrate using interferometric setup to decrease this background laser intensity, thus achieving higher S/N ratio and dye concentration detection sensitivity in SE microscopy.
© (2014) COPYRIGHT Society of Photo-Optical Instrumentation Engineers (SPIE). Downloading of the abstract is permitted for personal use only.
Shen-Shou Max Chung, Jia-Hui Deng, Po-Lin Lin, and Fu-Jen Kao "Enhancing stimulated emission-based fluorescence detection with interferometric setup", Proc. SPIE 8948, Multiphoton Microscopy in the Biomedical Sciences XIV, 89481T (28 February 2014); https://doi.org/10.1117/12.2042085
Advertisement
Advertisement
RIGHTS & PERMISSIONS
Get copyright permission  Get copyright permission on Copyright Marketplace
KEYWORDS
Laser beam diagnostics

Destructive interference

Interferometry

Signal detection

Luminescence

Fluorescence lifetime imaging

Mirrors

Back to Top