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We demonstrate the use of SCAPE microscopy to image both neural activity via GCaMP and vascular hemodynamics in the awake behaving mouse brain at 10-20 volumes per second with cellular resolution over large fields of view. The performance of SCAPE is compared to in-vivo two-photon microscopy.

Original publication

DOI

10.1364/brain.2015.brm2b.3

Type

Conference paper

Publication Date

06/04/2015