Extended two-photon microscopy in live samples with Bessel beams: Steadier focus, faster volume scans, and simpler stereoscopic imaging

Frontiers in Cellular Neuroscience

Volumn 8, Issue MAY, 2014, Pages

  Thériault, Gabrielle ^a,b   Cottet, Martin ^b   Castonguay, Annie ^b   McCarthy, Nathalie ^a,b   De Koninck, Yves ^a,b  

^a UNIVERSITÉ LAVAL   (Canada)

^b CENTRE DE RECHERCHE DE L INSTITUT UNIVERSITAIRE EN SANTÉ MENTALE DE QUÉBEC   (Canada)

Author keywords

3D imaging; Axicon; Cellular imaging; Depth of field; Functional calcium imaging; Nondiffractive beam; Nonlinear microscopy; Temporal resolution

Indexed keywords

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; BLEACHING; BRAIN CORTEX; BRAIN SLICE; CELL CULTURE; CONTROLLED STUDY; DENDRITE; EXCITATION; FLUORESCENCE MICROSCOPY; IMAGING; LASER; LENS; MEASUREMENT ERROR; MOUSE; NERVE CELL GROWTH; NEUROSCIENCE; NONHUMAN; OPTICAL RESOLUTION; SIGNAL NOISE RATIO; SPINAL GANGLION; STEREOMICROSCOPY; STEREOSCOPIC IMAGING; THREE DIMENSIONAL IMAGING; TIME LAPSE IMAGING; VISUAL SYSTEM;

EID: 84901286450     PISSN: 16625102     EISSN: None     Source Type: Journal    
DOI: 10.3389/fncel.2014.00139     Document Type: Article

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