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

Appelhans et al., 2017 - Google Patents

Single molecule tracking and localization of mitochondrial protein complexes in live cells

Appelhans et al., 2017

Document ID
9597096861019995540
Author
Appelhans T
Busch K
Publication year
Publication venue
Mitochondria: Practical Protocols

External Links

Snippet

Mitochondria are the power plant of most non-green eukaryotic cells. An understanding of their function and regulation is only possible with the knowledge of the spatiotemporal dynamics of their proteins. Mitochondrial membrane proteins involved in diverse functions …
Continue reading at link.springer.com (other versions)

Classifications

    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N21/00Investigating or analysing materials by the use of optical means, i.e. using infra-red, visible or ultra-violet light
    • G01N21/62Systems in which the material investigated is excited whereby it emits light or causes a change in wavelength of the incident light
    • G01N21/63Systems in which the material investigated is excited whereby it emits light or causes a change in wavelength of the incident light optically excited
    • G01N21/64Fluorescence; Phosphorescence
    • G01N21/645Specially adapted constructive features of fluorimeters
    • G01N21/6456Spatial resolved fluorescence measurements; Imaging
    • G01N21/6458Fluorescence microscopy
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N21/00Investigating or analysing materials by the use of optical means, i.e. using infra-red, visible or ultra-violet light
    • G01N21/62Systems in which the material investigated is excited whereby it emits light or causes a change in wavelength of the incident light
    • G01N21/63Systems in which the material investigated is excited whereby it emits light or causes a change in wavelength of the incident light optically excited
    • G01N21/64Fluorescence; Phosphorescence
    • G01N21/6428Measuring fluorescence of fluorescent products of reactions or of fluorochrome labelled reactive substances, e.g. measuring quenching effects, using measuring "optrodes"
    • G01N2021/6439Measuring 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
    • G01N2021/6441Measuring 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
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N21/00Investigating or analysing materials by the use of optical means, i.e. using infra-red, visible or ultra-violet light
    • G01N21/62Systems in which the material investigated is excited whereby it emits light or causes a change in wavelength of the incident light
    • G01N21/63Systems in which the material investigated is excited whereby it emits light or causes a change in wavelength of the incident light optically excited
    • G01N21/65Raman scattering
    • G01N2021/653Coherent methods [CARS]
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N33/00Investigating or analysing materials by specific methods not covered by the preceding groups
    • G01N33/48Investigating or analysing materials by specific methods not covered by the preceding groups biological material, e.g. blood, urine; Haemocytometers
    • G01N33/50Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
    • G01N33/58Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving labelled substances
    • G01N33/582Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving labelled substances with fluorescent label
    • GPHYSICS
    • G02OPTICS
    • G02BOPTICAL ELEMENTS, SYSTEMS, OR APPARATUS
    • G02B21/00Microscopes
    • G02B21/16Microscopes adapted for ultra-violet illumination; Fluorescence microscopes
    • GPHYSICS
    • G02OPTICS
    • G02BOPTICAL ELEMENTS, SYSTEMS, OR APPARATUS
    • G02B21/00Microscopes
    • G02B21/0004Microscopes specially adapted for specific applications
    • G02B21/002Scanning microscopes
    • G02B21/0024Confocal scanning microscopes (CSOMs) or confocal "macroscopes"; Accessories which are not restricted to use with CSOMs, e.g. sample holders
    • G02B21/0052Optical details of the image generation
    • G02B21/0076Optical details of the image generation arrangements using fluorescence or luminescence
    • GPHYSICS
    • G02OPTICS
    • G02BOPTICAL ELEMENTS, SYSTEMS, OR APPARATUS
    • G02B21/00Microscopes
    • G02B21/36Microscopes arranged for photographic purposes or projection purposes or digital imaging or video purposes including associated control and data processing arrangements
    • G02B21/365Control or image processing arrangements for digital or video microscopes

Similar Documents

Publication Publication Date Title
Thiele et al. Confocal fluorescence-lifetime single-molecule localization microscopy
Schermelleh et al. Super-resolution microscopy demystified
Appelhans et al. Single molecule tracking and localization of mitochondrial protein complexes in live cells
Tuijtel et al. Correlative cryo super-resolution light and electron microscopy on mammalian cells using fluorescent proteins
Gao et al. Expansion stimulated emission depletion microscopy (ExSTED)
Turkowyd et al. From single molecules to life: microscopy at the nanoscale
Wollman et al. From Animaculum to single molecules: 300 years of the light microscope
Komis et al. Advances in imaging plant cell dynamics
Frei et al. Photoactivation of silicon rhodamines via a light-induced protonation
Odermatt et al. High-resolution correlative microscopy: bridging the gap between single molecule localization microscopy and atomic force microscopy
van de Linde et al. Subdiffraction-resolution fluorescence imaging of proteins in the mitochondrial inner membrane with photoswitchable fluorophores
Auer et al. Nanometer‐scale Multiplexed Super‐Resolution Imaging with an Economic 3D‐DNA‐PAINT Microscope
Requejo-Isidro Fluorescence nanoscopy. Methods and applications
Oddone et al. Super‐resolution imaging with stochastic single‐molecule localization: concepts, technical developments, and biological applications
Yao et al. Multiplexed bioluminescence microscopy via phasor analysis
Liu et al. Fluorescent bioconjugates for super-resolution optical nanoscopy
Whelan et al. Focus on super-resolution imaging with direct stochastic optical reconstruction microscopy (dSTORM)
Sekhar et al. A cell-permeant small molecule for the super-resolution imaging of the endoplasmic reticulum in live cells
Li et al. Prospects for fluorescence nanoscopy
Appelhans et al. Multi-color localization microscopy of single membrane proteins in organelles of live mammalian cells
DʼEste et al. Advancing cell biology with nanoscale fluorescence imaging: essential practical considerations
Herrmannsdörfer et al. 3D d STORM imaging of fixed brain tissue
Abdelsayed et al. An optimized buffer for repeatable multicolor STORM
Halabi et al. A Simple Probe for Super‐Resolution Imaging of the Endoplasmic Reticulum in Living Cells
Gardini et al. Three-dimensional tracking of quantum dot-conjugated molecules in living cells