Background Rejection in Two-Photon Fluorescence Image Scanning Microscopy
We discuss the properties of signal strength and integrated intensity in two-photon excitation confocal microscopy and image scanning microscopy. The resolution, optical sectioning and background rejection are all improved over nonconfocal two-photon microscopy. Replacing the pinhole of confocal two...
| Published in: | Photonics |
|---|---|
| Main Authors: | , , , , , , , |
| Format: | Article |
| Language: | English |
| Published: |
MDPI AG
2023-05-01
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| Subjects: | |
| Online Access: | https://www.mdpi.com/2304-6732/10/5/601 |
