Fluorescence radial fluctuation enables two-photon super-resolution microscopy
Despite recent improvements in microscopy, it is still difficult to apply super-resolution microscopy for deep imaging due to the deterioration of light convergence properties in thick specimens. As a strategy to avoid such optical limitations for deep super-resolution imaging, we focused on super-r...
Main Authors: | Motosuke Tsutsumi, Taiga Takahashi, Kentaro Kobayashi, Tomomi Nemoto |
---|---|
Format: | Article |
Language: | English |
Published: |
Frontiers Media S.A.
2023-10-01
|
Series: | Frontiers in Cellular Neuroscience |
Subjects: | |
Online Access: | https://www.frontiersin.org/articles/10.3389/fncel.2023.1243633/full |
Similar Items
-
Dynamic Structure of Yeast Septin by Fast Fluctuation-Enhanced Structured Illumination Microscopy
by: Longfang Yao, et al.
Published: (2021-10-01) -
Real-Time Polarization-Resolved Imaging of Living Tissues Based on Two-Photon Excitation Spinning-Disk Confocal Microscopy
by: Ai Goto, et al.
Published: (2019-04-01) -
Improving two-photon excitation microscopy for sharper and faster biological imaging
by: Kohei Otomo, et al.
Published: (2023-02-01) -
Protocol for constructing an extensive cranial window utilizing a PEO-CYTOP nanosheet for in vivo wide-field imaging of the mouse brain
by: Taiga Takahashi, et al.
Published: (2021-06-01) -
Three-Dimensional Analysis of Cell Division Orientation in Epidermal Basal Layer Using Intravital Two-Photon Microscopy.
by: Sari Ipponjima, et al.
Published: (2016-01-01)