Smith et al., 2014 - Google Patents
Quantitatively imaging chromosomes by correlated cryo-fluorescence and soft x-ray tomographiesSmith et al., 2014
View HTML- Document ID
- 12230079716706576048
- Author
- Smith E
- McDermott G
- Do M
- Leung K
- Panning B
- Le Gros M
- Larabell C
- Publication year
- Publication venue
- Biophysical journal
External Links
Snippet
Soft x-ray tomography (SXT) is increasingly being recognized as a valuable method for visualizing and quantifying the ultrastructure of cryopreserved cells. Here, we describe the combination of SXT with cryogenic confocal fluorescence tomography (CFT). This correlativeĀ ā¦
- 238000003384 imaging method 0 title description 31
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
- 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
- G01N21/6428—Measuring fluorescence of fluorescent products of reactions or of fluorochrome labelled reactive substances, e.g. measuring quenching effects, using measuring "optrodes"
-
- 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
- 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
- G02B21/34—Microscope slides, e.g. mounting specimens on microscope slides
-
- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS, OR APPARATUS
- G02B21/00—Microscopes
- G02B21/02—Objectives
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| Smith et al. | Quantitatively imaging chromosomes by correlated cryo-fluorescence and soft x-ray tomographies | |
| Gorelick et al. | PIE-scope, integrated cryo-correlative light and FIB/SEM microscopy | |
| Laine et al. | High-fidelity 3D live-cell nanoscopy through data-driven enhanced super-resolution radial fluctuation | |
| Wu et al. | Multi-scale 3D cryo-correlative microscopy for vitrified cells | |
| Wollman et al. | From Animaculum to single molecules: 300 years of the light microscope | |
| Thorn | A quick guide to light microscopy in cell biology | |
| Kraus et al. | Quantitative 3D structured illumination microscopy of nuclear structures | |
| Neu et al. | Innovative techniques, sensors, and approaches for imaging biofilms at different scales | |
| Fernandez et al. | Imaging plant growth in 4D: robust tissue reconstruction and lineaging at cell resolution | |
| McIntosh et al. | New views of cells in 3D: an introduction to electron tomography | |
| Legant et al. | High-density three-dimensional localization microscopy across large volumes | |
| Sharpe | Optical projection tomography | |
| Bharat et al. | Correlative microscopy of vitreous sections provides insights into BAR-domain organization in situ | |
| Yamashita et al. | Three-dimensional tracking of plus-tips by lattice light-sheet microscopy permits the quantification of microtubule growth trajectories within the mitotic apparatus | |
| Markert et al. | Filling the gap: adding super-resolution to array tomography for correlated ultrastructural and molecular identification of electrical synapses at the C. elegans connectome | |
| Strobl et al. | Improving your four-dimensional image: traveling through a decade of light-sheet-based fluorescence microscopy research | |
| Gell et al. | TIRF microscopy evanescent field calibration using tilted fluorescent microtubules | |
| Yu et al. | Nanoscale three-dimensional single particle tracking by light-sheet-based double-helix point spread function microscopy | |
| Birk | Super-resolution microscopy of chromatin | |
| Kittisopikul et al. | Quantitative analysis of nuclear lamins imaged by super-resolution light microscopy | |
| Siegmund et al. | isoSTED microscopy with water-immersion lenses and background reduction | |
| Stauffer et al. | Diffusion through a liquid crystalline compartment regulates meiotic recombination | |
| Miao et al. | Dual-modal three-dimensional imaging of single cells with isometric high resolution using an optical projection tomography microscope | |
| Smith et al. | Correlative microscopy methods that maximize specimen fidelity and data completeness, and improve molecular localization capabilities | |
| Nakatani et al. | Long-axial-range double-helix point spread functions for 3D volumetric super-resolution imaging |