STED microscopy—super-resolution bio-imaging utilizing a stimulated emission depletion
Kohei Otomo, Terumasa Hibi, Yuichi Kozawa, Tomomi Nemoto
Abstract
Kohei Otomo, Terumasa Hibi, Yuichi Kozawa, Tomomi Nemoto
Abstract
One of the most popular super-resolution microscopies that breaks the diffraction barrier is stimulated emission depletion (STED) microscopy. As the optical set-up of STED microscopy is based on a laser scanning microscopy (LSM) system, it potentially has several merits of LSM like confocal or two-photon excitation LSM. In this article, we first describe the principles of STED microscopy and then describe the features of our newly developed two-photon excitation STED microscopy. On the basis of our recent results and those of other researchers, we conclude by discussing future research and new technologies in this field.
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One of the most popular super-resolution microscopies that breaks the diffraction barrier is stimulated emission depletion (STED) microscopy. As the optical set-up of STED microscopy is based on a laser scanning microscopy (LSM) system, it potentially has several merits of LSM like confocal or two-photon excitation LSM. In this article, we first describe the principles of STED microscopy and then describe the features of our newly developed two-photon excitation STED microscopy. On the basis of our recent results and those of other researchers, we conclude by discussing future research and new technologies in this field.
Key concepts: STED microscopy, Microscopy, Stimulated emission, Super-resolution microscopy, Confocal microscopy, Two-photon excitation microscopy, Optics, Confocal