TY - JOUR
T1 - STED microscopy – super-resolution bio-imaging utilizing a stimulated emission depletion
AU - Otomo, Kohei
AU - Hibi, Terumasa
AU - Kozawa, Yuichi
AU - Nemoto, Tomomi
N1 - Publisher Copyright:
© The Author 2015. Published by Oxford University Press on behalf of The Japanese Society of Microscopy. All rights reserved.
PY - 2015/8/1
Y1 - 2015/8/1
N2 - 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.
AB - 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.
KW - Liquid crystal devices
KW - Optical vortex
KW - Two-photon microscopy
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U2 - 10.1093/jmicro/dfv036
DO - 10.1093/jmicro/dfv036
M3 - Review article
AN - SCOPUS:84939781924
SN - 2050-5698
VL - 64
SP - 227
EP - 236
JO - Microscopy (Oxford, England)
JF - Microscopy (Oxford, England)
IS - 4
ER -