Presentation
16 March 2023 Advancing low flux in vivo two-photon voltage imaging (Conference Presentation)
Author Affiliations +
Abstract
Monitoring spiking activity across large neuronal populations at behaviorally relevant timescales is critical for understanding neural circuit function. Voltage imaging requires kilohertz sampling rates which reduce fluorescence detection to near shot noise levels. High-photon flux excitation can overcome photon-limited shot noise but photo-bleaching and photo-damage restrict the number and duration of simultaneously imaged neurons. We investigated an alternative approach aimed at low two-photon flux, voltage imaging below the shot noise limit with the goal of achieving simultaneous high-speed, deep-tissue imaging of more than one hundred densely labeled neurons over one hour in awake behaving mice.
Conference Presentation
© (2023) COPYRIGHT Society of Photo-Optical Instrumentation Engineers (SPIE). Downloading of the abstract is permitted for personal use only.
Jerry Chen "Advancing low flux in vivo two-photon voltage imaging (Conference Presentation)", Proc. SPIE PC12390, High-Speed Biomedical Imaging and Spectroscopy VIII, PC1239007 (16 March 2023); https://doi.org/10.1117/12.2656201
Advertisement
Advertisement
KEYWORDS
In vivo imaging

Two photon imaging

Imaging systems

Microscopes

Neurons

Denoising

Fluorescence spectroscopy

RELATED CONTENT


Back to Top