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

Two-photon microscopy has revolutionized functional cellular imaging in tissue, but although the highly confined depth of field (DOF) of standard set-ups yields great optical sectioning, it also limits imaging speed in volume samples and ease of use. For this reason, we recently presented a simple a...

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Detalles Bibliográficos
Autores principales: Thériault, Gabrielle, Cottet, Martin, Castonguay, Annie, McCarthy, Nathalie, De Koninck, Yves
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2014
Materias:
Neuroscience
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4032997/
https://www.ncbi.nlm.nih.gov/pubmed/24904284
http://dx.doi.org/10.3389/fncel.2014.00139

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4032997/
https://www.ncbi.nlm.nih.gov/pubmed/24904284
http://dx.doi.org/10.3389/fncel.2014.00139

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