Abstract
We integrated two-photon microscopy (TPM), second harmonic imaging microscopy (SHIM), near-infrared fluorescence microscopy (NIRF), confocal laser scanning microscopy (CLSM), and fluorescence lifetime imaging microscopy (FLIM) in one microscope system. Using our microscope system, five different images were obtained simultaneously.
Original language | English |
---|---|
Title of host publication | Advances in Microscopic Imaging II |
Editors | Emmanuel Beaurepaire, Francesco Saverio Pavone |
Publisher | SPIE |
ISBN (Electronic) | 9781510628458 |
DOIs | |
Publication status | Published - 2019 |
Event | Advances in Microscopic Imaging II 2019 - Munich, Germany Duration: 2019 Jun 26 → 2019 Jun 27 |
Publication series
Name | Progress in Biomedical Optics and Imaging - Proceedings of SPIE |
---|---|
Volume | 11076 |
ISSN (Print) | 1605-7422 |
Conference
Conference | Advances in Microscopic Imaging II 2019 |
---|---|
Country/Territory | Germany |
City | Munich |
Period | 19/6/26 → 19/6/27 |
Bibliographical note
Publisher Copyright:© 2019 SPIE.
Keywords
- Confocal laser scanning microscopy
- Fluorescence lifetime imaging microscopy
- Multimodal optical microscope
- Near infra-red fluorescence
- Second harmonic generation
- Two-photon microscopy
ASJC Scopus subject areas
- Electronic, Optical and Magnetic Materials
- Atomic and Molecular Physics, and Optics
- Radiology Nuclear Medicine and imaging
- Biomaterials