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

Bates et al., 2013 - Google Patents

Stochastic optical reconstruction microscopy (STORM): a method for superresolution fluorescence imaging

Bates et al., 2013

View PDF
Document ID
15457598943314329274
Author
Bates M
Jones S
Zhuang X
Publication year
Publication venue
Cold Spring Harbor Protocols

External Links

Snippet

The relatively low spatial resolution of the optical microscope presents significant limitations for the observation of biological ultrastructure. Subcellular structures and molecular complexes essential for biological function exist on length scales from nanometers to …
Continue reading at citeseerx.ist.psu.edu (PDF) (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"
    • 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
    • G02B21/0004—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
    • 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
    • G01N21/17—Systems in which incident light is modified in accordance with the properties of the material investigated
    • 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
    • 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
    • G02B26/00—Optical devices or arrangements using movable or deformable optical elements for controlling the intensity, colour, phase, polarisation or direction of light, e.g. switching, gating, modulating

Similar Documents

Publication Publication Date Title
Bates et al. Stochastic optical reconstruction microscopy (STORM): a method for superresolution fluorescence imaging
Schermelleh et al. Super-resolution microscopy demystified
Thiele et al. Confocal fluorescence-lifetime single-molecule localization microscopy
Gould et al. Imaging biological structures with fluorescence photoactivation localization microscopy
Cutler et al. Multi-color quantum dot tracking using a high-speed hyperspectral line-scanning microscope
Hell et al. Diffraction-unlimited three-dimensional optical nanoscopy with opposing lenses
Hell Far-field optical nanoscopy
Grotjohann et al. rsEGFP2 enables fast RESOLFT nanoscopy of living cells
Sanderson et al. Fluorescence microscopy
Aquino et al. Two-color nanoscopy of three-dimensional volumes by 4Pi detection of stochastically switched fluorophores
Testa et al. Multicolor fluorescence nanoscopy in fixed and living cells by exciting conventional fluorophores with a single wavelength
Malkusch et al. Coordinate-based colocalization analysis of single-molecule localization microscopy data
Grant et al. High speed optically sectioned fluorescence lifetime imaging permits study of live cell signaling events
Requejo-Isidro Fluorescence nanoscopy. Methods and applications
Johnson et al. Total internal reflection fluorescence (TIRF) microscopy illuminator for improved imaging of cell surface events
Dempsey A user’s guide to localization-based super-resolution fluorescence imaging
Lee et al. Video-rate confocal microscopy for single-molecule imaging in live cells and superresolution fluorescence imaging
Reck-Peterson et al. Imaging single molecules using total internal reflection fluorescence microscopy (TIRFM)
Kanchanawong et al. Advances in light-based imaging of three-dimensional cellular ultrastructure
Nelson et al. Localization microscopy: mapping cellular dynamics with single molecules
Hess et al. Ultrahigh resolution imaging of biomolecules by fluorescence photoactivation localization microscopy
Rai et al. The basics of confocal microscopy
Galiani et al. Super-resolution microscopy and studies of peroxisomes
Siegmund et al. isoSTED microscopy with water-immersion lenses and background reduction
Adams et al. Signal analysis of total internal reflection fluorescent speckle microscopy (TIR‐FSM) and wide‐field epi‐fluorescence FSM of the actin cytoskeleton and focal adhesions in living cells