
M47 - FLIM - Picoquant Fluorescent Lifetime Imaging Microscope
System Description
FLIM measures the total fluorescence lifetime of fluorophores (as in, how long on average a fluorophore stays in its excited state following excitation from a short excitation light pulse). This can give you a wealth of information on the fluorophore’s local chemical and physical environment (“local” meaning nanometer scale!). It can also be used to study translational and rotational behaviour of the fluorophores and their relative orientations as well as orientational dynamics (thereby allowing an estimation of the respective properties of the attached molecules). It also allows highly accurate FRET imaging, eliminating the crosstalk and/or bleaching problems inherent to standard ratiometric FRET imaging, and it provides an elegant tool for (time-resolved) anisotropy measurements
FLIM approach allows high accuracy FRET imaging, eliminating the crosstalk and/or bleaching problems inherent to standard ratiometric FRET imaging.
This microscope, although officially belonging to CSF, can be used by IMP-IMBA-GMI users as any other system of the BioOptics facility, without any extra costs. The system is situated in VBC6, room E32A.
Microscope frame
Olympus iX71 inverted microscope frame
Excitation
Laser: 440 nm, 510 nm
Objective lenses (Olympus)
PL 20 x PlanAchromat Objektiv, NA = 0.4
PL 40 x PlanAchromat Objektiv, NA = 0.65
UPLSAPO 60 x Ultra-Planapochromat, NA = 1.2 (water immersion)
PLAPON 60 x Plan Apo, NA = 1.42 (oil immersion)
Filters & Beam Splitters
These vary according to the experimental demands. Any common (and many uncommon) filter / beamsplitter combinations can be installed.
Detector
Hybrid Photomultiplier Detection Assembly with < 50 ps time resolution
Analysis Software
SymPhoTime 64 (more details on the Picoquant webpage)
External Links
More information on TCSPC theory and data analysis available on a Picoquant Wikipage
Further information also available on the CSF Homepage
Reservation & Training
If you wish to use (or learn more about) the FLIM system, please send an email to microscopy(at)imp.ac.at in order to arrange the training.