[go: up one dir, main page]
More Web Proxy on the site http://driver.im/

Herrmannsdörfer et al., 2017 - Google Patents

3D d STORM imaging of fixed brain tissue

Herrmannsdörfer et al., 2017

Document ID
2929047661832832523
Author
Herrmannsdörfer F
Flottmann B
Nanguneri S
Venkataramani V
Horstmann H
Kuner T
Heilemann M
Publication year
Publication venue
Synapse Development: Methods and Protocols

External Links

Snippet

Central nervous system tissue contains a high density of synapses each composed of an intricate molecular machinery mediating precise transmission of information. Deciphering the molecular nanostructure of pre-and postsynaptic specializations within such a complex …
Continue reading at link.springer.com (other versions)

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"
    • G01N2021/6439—Measuring fluorescence of fluorescent products of reactions or of fluorochrome labelled reactive substances, e.g. measuring quenching effects, using measuring "optrodes" with indicators, stains, dyes, tags, labels, marks
    • G01N2021/6441—Measuring fluorescence of fluorescent products of reactions or of fluorochrome labelled reactive substances, e.g. measuring quenching effects, using measuring "optrodes" with indicators, stains, dyes, tags, labels, marks with two or more labels
    • 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
    • G02B21/16—Microscopes adapted for ultra-violet illumination; Fluorescence 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
    • G02B21/0076—Optical details of the image generation arrangements using fluorescence or luminescence
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N33/00—Investigating or analysing materials by specific methods not covered by the preceding groups
    • G01N33/48—Investigating or analysing materials by specific methods not covered by the preceding groups biological material, e.g. blood, urine; Haemocytometers
    • G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
    • G—PHYSICS
    • G02—OPTICS
    • G02B—OPTICAL ELEMENTS, SYSTEMS, OR APPARATUS
    • G02B21/00—Microscopes
    • G02B21/02—Objectives
    • G—PHYSICS
    • G02—OPTICS
    • G02B—OPTICAL ELEMENTS, SYSTEMS, OR APPARATUS
    • G02B21/00—Microscopes
    • G02B21/24—Base structure

Similar Documents

Publication Publication Date Title
Liu et al. Super-resolution microscopy for structural cell biology
Tuijtel et al. Correlative cryo super-resolution light and electron microscopy on mammalian cells using fluorescent proteins
Lelek et al. Single-molecule localization microscopy
Jouchet et al. Nanometric axial localization of single fluorescent molecules with modulated excitation
Diekmann et al. Optimizing imaging speed and excitation intensity for single-molecule localization microscopy
Xu et al. Stochastic optical reconstruction microscopy (STORM)
Turkowyd et al. From single molecules to life: microscopy at the nanoscale
Baddeley et al. 4D super-resolution microscopy with conventional fluorophores and single wavelength excitation in optically thick cells and tissues
Wang et al. Solid immersion microscopy images cells under cryogenic conditions with 12 nm resolution
Bates et al. Stochastic optical reconstruction microscopy (STORM): a method for superresolution fluorescence imaging
Endesfelder et al. Direct stochastic optical reconstruction microscopy (d STORM)
York et al. Confined activation and subdiffractive localization enables whole-cell PALM with genetically expressed probes
Cabriel et al. Combining 3D single molecule localization strategies for reproducible bioimaging
MacDonald et al. Does super-resolution fluorescence microscopy obsolete previous microscopic approaches to protein co-localization?
Middendorff et al. Isotropic 3D Nanoscopy based on single emitter switching
Birk Super-resolution microscopy: a practical guide
Herrmannsdörfer et al. 3D d STORM imaging of fixed brain tissue
Requejo-Isidro Fluorescence nanoscopy. Methods and applications
Babcock Multiplane and spectrally-resolved single molecule localization microscopy with industrial grade CMOS cameras
Tian et al. Cryogenic superresolution correlative light and electron microscopy on the frontier of subcellular imaging
Mohammadian et al. Integrated super resolution fluorescence microscopy and transmission electron microscopy
Reilly et al. Advances in confocal microscopy and selected applications
Tuijtel et al. Inducing fluorescence of uranyl acetate as a dual-purpose contrast agent for correlative light-electron microscopy with nanometre precision
Galiani et al. Super-resolution microscopy and studies of peroxisomes
McEvoy et al. Q&A: Single-molecule localization microscopy for biological imaging