Abstract
Two-photon microscopy is a powerful technique for in vivo imaging, due to its high penetration depth and axial sectioning. Usually excitation wavelengths in the near infrared are used. However, most fluorescence techniques for live cell imaging require labeling with exogenous fluorophores. It has been shown that shorter wavelengths can be used to excite the autofluorescence of endogenous proteins, e.g. tryptophan [1].
| Original language | English |
|---|---|
| Title of host publication | 2019 Conference on Lasers and Electro-Optics Europe & European Quantum Electronics Conference (CLEO/Europe-EQEC) |
| Publisher | IEEE |
| Publication date | 06.2019 |
| Article number | 8872571 |
| ISBN (Print) | 978-1-7281-0470-6 |
| ISBN (Electronic) | 978-1-7281-0469-0 |
| DOIs | |
| Publication status | Published - 06.2019 |
| Event | 2019 Conference on Lasers and Electro-Optics Europe and European Quantum Electronics Conference - Munich, Germany Duration: 23.06.2019 → 27.06.2019 Conference number: 152846 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
-
SDG 9 Industry, Innovation, and Infrastructure
Research Areas and Centers
- Academic Focus: Biomedical Engineering
Fingerprint
Dive into the research topics of 'Sub-nanosecond pulsed fiber laser for 532nm two-photon excitation fluorescence (TPEF) microscopy of UV transitions'. Together they form a unique fingerprint.Cite this
- APA
- Author
- BIBTEX
- Harvard
- Standard
- RIS
- Vancouver