Fast live-cell conventional fluorophore nanoscopy with ImageJ through super-resolution radial fluctuations

Nature Communications

Volumn 7, Issue , 2016, Pages

  Gustafsson, Nils ^a   Culley, Siân ^a   Ashdown, George ^b   Owen, Dylan M ^b   Pereira, Pedro Matos ^a   Henriques, Ricardo ^a  

^a UNIVERSITY COLLEGE LONDON   (United Kingdom)

^b KING'S COLLEGE LONDON   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ANALYTICAL METHOD; DATA SET; IMAGE PROCESSING; MICROSCOPY; NANOTECHNOLOGY; RESOLUTION;

ALGORITHM; ANIMAL CELL; ARTICLE; COMPUTER MODEL; CONFOCAL MICROSCOPY; FEMALE; HUMAN; HUMAN CELL; ILLUMINATION; IMAGE ANALYSIS; IMAGE PROCESSING; IMAGING SOFTWARE; NANOIMAGING; NONHUMAN; PHOTOACTIVATED LOCALIZATION MICROSCOPY; SIGNAL NOISE RATIO; STOCHASTIC OPTICAL RECONSTRUCTION MICROSCOPY; SUPER RESOLUTION RADIAL FLUCTUATION; ANIMAL; CELL LINE; CHEMISTRY; DEVICES; FLUORESCENCE IMAGING; FLUORESCENCE MICROSCOPY; NANOTECHNOLOGY; PROCEDURES; RHESUS MONKEY; TIME FACTOR;

FLUORESCENT DYE; IONOPHORE;

ANIMALS; CELL LINE; FLUORESCENT DYES; HUMANS; IONOPHORES; MACACA MULATTA; MICROSCOPY, CONFOCAL; MICROSCOPY, FLUORESCENCE; NANOTECHNOLOGY; OPTICAL IMAGING; TIME FACTORS;

EID: 84982245157     PISSN: None     EISSN: 20411723     Source Type: Journal    
DOI: 10.1038/ncomms12471     Document Type: Article

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