High speed functional imaging with source localized multifocal two-photon microscopy

Multifocal two-photon microscopy (MTPM) increases imaging speed over single-focus scanning by parallelizing fluorescence excitation. The imaged fluorescence’s susceptibility to crosstalk, however, severely degrades contrast in scattering tissue. Here we present a source-localized MTPM scheme optimiz...

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Detalles Bibliográficos
Autores principales: Quicke, Peter, Reynolds, Stephanie, Neil, Mark, Knöpfel, Thomas, Schultz, Simon R., Foust, Amanda J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Optical Society of America 2018
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6191622/
https://www.ncbi.nlm.nih.gov/pubmed/30338147
http://dx.doi.org/10.1364/BOE.9.003678

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6191622/
https://www.ncbi.nlm.nih.gov/pubmed/30338147
http://dx.doi.org/10.1364/BOE.9.003678

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