Sun et al., 2023 - Google Patents
Fluorescence interference structured illumination microscopy for 3D morphology imaging with high axial resolutionSun et al., 2023
View PDF- Document ID
- 10828812708111299190
- Author
- Sun Y
- Zhu H
- Yin L
- Wu H
- Cai M
- Sun W
- Xu Y
- Yang X
- Han J
- Liu W
- Han Y
- Hao X
- Zhou R
- Kuang C
- Liu X
- Publication year
- Publication venue
- Advanced Photonics
External Links
Snippet
Imaging three-dimensional, subcellular structures with high axial resolution has always been the core purpose of fluorescence microscopy. However, trade-offs exist between axial resolution and other important technical indicators, such as temporal resolution, optical …
Classifications
-
- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS, OR APPARATUS
- G02B21/00—Microscopes
- G02B21/0004—Microscopes specially adapted for specific applications
- G02B21/002—Scanning microscopes
- G02B21/0024—Confocal scanning microscopes (CSOMs) or confocal "macroscopes"; Accessories which are not restricted to use with CSOMs, e.g. sample holders
- G02B21/0052—Optical details of the image generation
- G02B21/0076—Optical details of the image generation arrangements using fluorescence or luminescence
-
- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS, OR APPARATUS
- G02B21/00—Microscopes
- G02B21/0004—Microscopes specially adapted for specific applications
- G02B21/002—Scanning microscopes
- G02B21/0024—Confocal scanning microscopes (CSOMs) or confocal "macroscopes"; Accessories which are not restricted to use with CSOMs, e.g. sample holders
- G02B21/0028—Confocal scanning microscopes (CSOMs) or confocal "macroscopes"; Accessories which are not restricted to use with CSOMs, e.g. sample holders specially adapted for specific applications, e.g. for endoscopes, ophthalmoscopes, attachments to conventional microscopes
-
- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS, OR APPARATUS
- G02B21/00—Microscopes
- G02B21/36—Microscopes arranged for photographic purposes or projection purposes or digital imaging or video purposes including associated control and data processing arrangements
- G02B21/365—Control or image processing arrangements for digital or video microscopes
- G02B21/367—Control or image processing arrangements for digital or video microscopes providing an output produced by processing a plurality of individual source images, e.g. image tiling, montage, composite images, depth sectioning, image comparison
-
- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS, OR APPARATUS
- G02B21/00—Microscopes
- G02B21/0004—Microscopes specially adapted for specific applications
- G02B21/002—Scanning microscopes
- G02B21/0024—Confocal scanning microscopes (CSOMs) or confocal "macroscopes"; Accessories which are not restricted to use with CSOMs, e.g. sample holders
- G02B21/0052—Optical details of the image generation
- G02B21/0072—Optical details of the image generation details concerning resolution or correction, including general design of CSOM objectives
-
- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS, OR APPARATUS
- G02B21/00—Microscopes
- G02B21/16—Microscopes adapted for ultra-violet illumination; Fluorescence microscopes
-
- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS, OR APPARATUS
- G02B27/00—Other optical systems; Other optical apparatus
- G02B27/58—Optics for apodization or superresolution; Optical synthetic aperture systems
-
- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS, OR APPARATUS
- G02B21/00—Microscopes
- G02B21/06—Means for illuminating specimens
- G02B21/08—Condensers
-
- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS, OR APPARATUS
- G02B3/00—Simple or compound lenses
-
- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS, OR APPARATUS
- G02B5/00—Optical elements other than lenses
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| Park et al. | Review of bio-optical imaging systems with a high space-bandwidth product | |
| Booth et al. | Aberrations and adaptive optics in super-resolution microscopy | |
| Jiang et al. | Resolution-enhanced parallel coded ptychography for high-throughput optical imaging | |
| Aguet et al. | A maximum-likelihood formalism for sub-resolution axial localization of fluorescent nanoparticles | |
| Brunstein et al. | Full-field dual-color 100-nm super-resolution imaging reveals organization and dynamics of mitochondrial and ER networks | |
| Rogers et al. | Far-field unlabeled super-resolution imaging with superoscillatory illumination | |
| Sun et al. | Fluorescence interference structured illumination microscopy for 3D morphology imaging with high axial resolution | |
| Guan et al. | Polarization modulation with optical lock-in detection reveals universal fluorescence anisotropy of subcellular structures in live cells | |
| Attota | Through-focus or volumetric type of optical imaging methods: a review | |
| Cao et al. | Volumetric interferometric lattice light-sheet imaging | |
| Fan et al. | Wide-field anti-aliased quantitative differential phase contrast microscopy | |
| Zhao et al. | Advances in high-speed structured illumination microscopy | |
| Huttunen et al. | Label-free super-resolution with coherent nonlinear structured-illumination microscopy | |
| He et al. | Temporal compressive super-resolution microscopy at frame rate of 1200 frames per second and spatial resolution of 100 nm | |
| Li et al. | Rapid 3D image scanning microscopy with multi-spot excitation and double-helix point spread function detection | |
| Li et al. | High-speed autopolarization synchronization modulation three-dimensional structured illumination microscopy | |
| Wang et al. | Adaptive optics in super-resolution microscopy | |
| Birk et al. | Super-resolution microscopy with very large working distance by means of distributed aperture illumination | |
| Wang et al. | Hybrid multifocal structured illumination microscopy with enhanced lateral resolution and axial localization capability | |
| Ping et al. | Propagating-path uniformly scanned light sheet excitation microscopy for isotropic volumetric imaging of large specimens | |
| Miles et al. | On the complex point spread function in interferometric cross-polarisation microscopy | |
| Wen et al. | Structured illumination phase and fluorescence microscopy for bioimaging | |
| Temma et al. | Selective-plane-activation structured illumination microscopy | |
| Wang et al. | Double helix point spread function with variable spacing for precise 3D particle localization | |
| Barak et al. | Module for zooming in extended depth of focus in digital holographic microscopy |