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Fluorescence and confocal microscopes operating principle. Confocal microscopy, most frequently confocal laser scanning microscopy (CLSM) or laser scanning confocal microscopy (LSCM), is an optical imaging technique for increasing optical resolution and contrast of a micrograph by means of using a spatial pinhole to block out-of-focus light in image formation. [1]
Similar to confocal microscopy, the laser in CLE filtered by the pinhole excites the fluorescent dye through a beam splitter and objective lens. The fluorescent emission then follows similar paths into the detector. A pinhole is used to select emissions from the desired focal plane. Two categories of CLE exist, namely probe-based (pCLE) and the ...
Confocal microscope, a widely used variant of epifluorescent illumination that uses a scanning laser to illuminate a sample for fluorescence. Two-photon microscope , used to image fluorescence deeper in scattering media and reduce photobleaching, especially in living samples.
Endomicroscopy is a technique for obtaining histology-like images from inside the human body in real-time, [1] [2] [3] a process known as ‘optical biopsy’. [4] [5] It generally refers to fluorescence confocal microscopy, although multi-photon microscopy and optical coherence tomography have also been adapted for endoscopic use.
Confocal Raman imaging microscope Raman microscope. The Raman microscope is a laser-based microscopic device used to perform Raman spectroscopy. [1] The term MOLE (molecular optics laser examiner) is used to refer to the Raman-based microprobe. [1] The technique used is named after C. V. Raman, who discovered the scattering properties in ...
Edge filters are used for removal of all primary laser light. Resolution as low as 10 nm can be achieved using this technique. [citation needed] Near field infrared spectrometry and near-field dielectric microscopy [19] use near-field probes to combine sub-micron microscopy with localized IR spectroscopy. [25]