STED Microscopy
Department of NanoBiophotonics, Max Planck Institute for Biophysical Chemistry, Göttingen, Germany
Abstract
Far-field fluorescence microscopy is among the most frequently used methods in biomedical research today. Due to diffraction, it has long been subject to a limited spatial resolution but since the invention of stimulated emission depletion (STED) microscopy and subsequent high-resolution imaging techniques enables imaging at the nanoscale. Because STED microscopy is efficiently implemented using ultrashort pulsed lasers it has often been associated with complex setups and costly and high-maintenance laser systems. Recent developments in laser technology have allowed to design powerful, less complex and easy-to-operate STED microscopes which allow spatial resolutions down to 20 nm in 2D or 45 nm x 45 nm x 108 nm in 3D to be achieved. The broad spectrum of the supercontinuum sources permit the use of fluorescent markers across the visible spectrum. Also, multicolor operation is readily conceivable.
Keywords
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