Related Experiment Video
Updated: Jun 22, 2026
08:32
Conducting Multiple Imaging Modes with One Fluorescence Microscope
Published on: October 28, 2018
Measuring large numerical apertures by imaging the angular distribution of radiation of fluorescing molecules
Optics Express
|June 9, 2009
Abstract:
Exact knowledge of the numerical aperture is crucial in many applications using high-aperture objectives such as confocal microscopy, optical trapping, or advanced sub-wavelength imaging methods. We propose and apply a precise and straightforward method for measuring this fundamental parameter of microscope objectives with numerical apertures above unity. Our method exploits the peculiarities of the fluorescence emission of molecules at a glass/air interface.
Related Concept Videos
01:37Super-resolution Fluorescence Microscopy
Super-resolution fluorescence microscopy (SRFM) provides a better resolution than conventional fluorescence microscopy by reducing the point spread function (PSF). PSF is the light intensity distribution from a point that causes it to appear blurred. Due to PSF, each fluorescing point appears bigger than its actual size, and it is the PSF interference of nearby fluorophores that causes the blurred image. Various approaches to achieving higher resolution through SRFM have recently been developed.
01:18Imaging Biological Samples with Optical Microscopy
Optical microscopy uses optic principles to provide detailed images of samples. Antonie van Leeuwenhoek designed the first compound optical microscope in the 17th century to visualize blood cells, bacteria, and yeast cells. In 1830, Joseph Jackson Lister created an essentially modern light microscope. The 20th century saw the development of microscopes with enhanced magnification and resolution.
In optical microscopy, the specimen to be viewed is placed on a glass slide and clipped on the stage...
In optical microscopy, the specimen to be viewed is placed on a glass slide and clipped on the stage...
01:25Fluorescence and Phosphorescence: Instrumentation
Fluorometers and spectrofluorometers are two types of instruments used for measuring molecular fluorescence. These instruments differ in how they select excitation and emission wavelengths and the type of light sources they utilize. Fluorometers use absorption interference filters to choose excitation and emission wavelengths. The excitation source in a fluorometer is typically a low-pressure mercury vapor lamp that emits intense lines distributed throughout the ultraviolet and visible regions.