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Bennett Joins Till Photonics

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MUNICH, Germany, July 14, 2010 — Fluorescence microscopy systems provider Till Photonics GmbH announced recently the addition of Dr. Brian T. Bennett as its director of scientific business development for microscopy. Bennett began his career at the University of Massachusetts Medical School, where he obtained his PhD and published several articles on the recruitment of cancer-related proteins within a human nucleus. The first to use microscopy to study the localization of specific proteins, he has published articles that have been awarded the cover photo for the Journal of Cellular Biochemistry. He has also...Read full article

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    Published: July 2010
    Glossary
    fluorescence microscopy
    Fluorescence microscopy is a specialized optical imaging technique used in biology, chemistry, and materials science to visualize and study specimens that exhibit fluorescence. Fluorescence is the phenomenon where a substance absorbs light at one wavelength and emits light at a longer wavelength. In fluorescence microscopy, fluorescent dyes or proteins are used to label specific structures or molecules within a sample. The basic principles of fluorescence microscopy involve illuminating the...
    sted microscopy
    STED microscopy, or stimulated emission depletion microscopy, is a superresolution imaging technique in fluorescence microscopy that surpasses the diffraction limit, enabling the visualization of structures at the nanoscale level. This technique was developed to overcome the limitations imposed by the diffraction of light, which traditionally hindered the resolution of optical microscopy to a few hundred nanometers. Key features and principles of STED microscopy: Superresolution: STED...
    superresolution
    Superresolution refers to the enhancement or improvement of the spatial resolution beyond the conventional limits imposed by the diffraction of light. In the context of imaging, it is a set of techniques and algorithms that aim to achieve higher resolution images than what is traditionally possible using standard imaging systems. In conventional optical microscopy, the resolution is limited by the diffraction of light, a phenomenon described by Ernst Abbe's diffraction limit. This limit sets a...
    AmericasBasic ScienceBi-plane Fluorescent Photo-Activatable Localization MicroscopyBi-plane FPALMbiologicalBiophotonicsBrian BennettBusinesscancerEuropefluorescence microscopyfluorescentImagingiMICJournal of Cellular BiochemistryMark Tolbertmicroscope platformMicroscopynucleusOpticsproteinSTED microscopysuper-resolutionsuperresolutionsuperresolution imagingsuperresolution microscopyTILL PhotonicsTill-USAUniversity of MassachusettsUniversity of Utah

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