Colombelli et al., 2014 - Google Patents
Light sheet fluorescence microscopy applications for multicellular systemsColombelli et al., 2014
- Document ID
- 2386239820041501057
- Author
- Colombelli J
- Lorenzo C
- Publication year
- Publication venue
- Fluorescence Microscopy
External Links
Snippet
Progress in imaging technology ultimately and inevitably pushes the limits of current cell biology. The continuous development of new biological probes, the diversification in biophysical properties of the fluorescent proteins (eg, spectra combinations, optical …
- 238000000799 fluorescence microscopy 0 title abstract description 22
Classifications
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N21/00—Investigating or analysing materials by the use of optical means, i.e. using infra-red, visible or ultra-violet light
- G01N21/62—Systems in which the material investigated is excited whereby it emits light or causes a change in wavelength of the incident light
- G01N21/63—Systems in which the material investigated is excited whereby it emits light or causes a change in wavelength of the incident light optically excited
- G01N21/64—Fluorescence; Phosphorescence
- G01N21/645—Specially adapted constructive features of fluorimeters
- G01N21/6456—Spatial resolved fluorescence measurements; Imaging
- G01N21/6458—Fluorescence microscopy
-
- 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
- G02B21/36—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
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N21/00—Investigating or analysing materials by the use of optical means, i.e. using infra-red, visible or ultra-violet light
- G01N21/62—Systems in which the material investigated is excited whereby it emits light or causes a change in wavelength of the incident light
- G01N21/63—Systems in which the material investigated is excited whereby it emits light or causes a change in wavelength of the incident light optically excited
- G01N21/65—Raman scattering
- G01N2021/653—Coherent methods [CARS]
-
- 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
- G02B21/16—Microscopes adapted for ultra-violet illumination; Fluorescence microscopes
-
- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS, OR APPARATUS
- G02B21/00—Microscopes
- G02B21/06—Means for illuminating specimens
- G02B21/08—Condensers
- G02B21/10—Condensers affording dark-field illumination
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N15/00—Investigating characteristics of particles; Investigating permeability, pore-volume, or surface-area of porous materials
- G01N15/10—Investigating individual particles
- G01N15/14—Electro-optical investigation, e.g. flow cytometers
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| Olarte et al. | Light-sheet microscopy: a tutorial | |
| Stelzer et al. | Light sheet fluorescence microscopy | |
| Chen et al. | Three-dimensional residual channel attention networks denoise and sharpen fluorescence microscopy image volumes | |
| Chen et al. | UbasM: An effective balanced optical clearing method for intact biomedical imaging | |
| Huisken et al. | Selective plane illumination microscopy techniques in developmental biology | |
| Weber et al. | Light sheet microscopy | |
| Medeiros et al. | Confocal multiview light-sheet microscopy | |
| Keller et al. | Light sheet microscopy of living or cleared specimens | |
| Chhetri et al. | Whole-animal functional and developmental imaging with isotropic spatial resolution | |
| Duocastella et al. | Fast inertia-free volumetric light-sheet microscope | |
| Poola et al. | Light sheet microscopy for histopathology applications | |
| Tomer et al. | Shedding light on the system: studying embryonic development with light sheet microscopy | |
| Reynaud et al. | Light sheet‐based fluorescence microscopy: more dimensions, more photons, and less photodamage | |
| Wu et al. | Spatially isotropic four-dimensional imaging with dual-view plane illumination microscopy | |
| Tomer et al. | Quantitative high-speed imaging of entire developing embryos with simultaneous multiview light-sheet microscopy | |
| US10746981B2 (en) | Methods and devices for imaging large intact tissue samples | |
| Pampaloni et al. | Light sheet-based fluorescence microscopy (LSFM) for the quantitative imaging of cells and tissues | |
| Fang et al. | Minutes-timescale 3D isotropic imaging of entire organs at subcellular resolution by content-aware compressed-sensing light-sheet microscopy | |
| Gualda et al. | Three‐dimensional imaging flow cytometry through light‐sheet fluorescence microscopy | |
| Keller | In vivo imaging of zebrafish embryogenesis | |
| Andilla et al. | Imaging tissue-mimic with light sheet microscopy: A comparative guideline | |
| Elisa et al. | Technical implementations of light sheet microscopy | |
| Swoger et al. | Light-sheet-based fluorescence microscopy for three-dimensional imaging of biological samples | |
| de Medeiros et al. | Light-sheet imaging of mammalian development | |
| Strobl et al. | Improving your four-dimensional image: traveling through a decade of light-sheet-based fluorescence microscopy research |