Philipp Lamminger

Doktorand / PhD-Student


BMO
Universität zu Lübeck
Maria-Goeppert-Str. 1
23562 Lübeck

Gebäude MFC1, Raum 1

Email:
Phone:
+49 (0)451 3101 3229
Fax:
+49 (0)451 3101 3233

Link zur AG-Huber Seite


Publikationen

2019

  • Weng, D; Hakert, H; Blömker, T; Kolb, JP; Strauch, M; Eibl, M; Lamminger, P; Karpf, S and Huber, R: Sub-Nanosecond Pulsed Fiber Laser for 532nm Two-Photon Excitation Fluorescence (TPEF) Microscopy of UV transitions. 2019 Conference on Lasers and Electro-Optics Europe and European Quantum Electronics Conference, in 2019 Conference on Lasers and Electro-Optics Europe and European Quantum Electronics Conference, pp. ch_9_3, Optical Society of America, 2019
    BibTeX Link
    @inproceedings{Weng:19,
    author = {Weng, D; Hakert, H; Bl\"{o}mker, T; Kolb, JP; Strauch, M; Eibl, M; Lamminger, P; Karpf, S and Huber, R},
    booktitle = {2019 Conference on Lasers and Electro-Optics Europe and European Quantum Electronics Conference},
    journal = {2019 Conference on Lasers and Electro-Optics Europe and European Quantum Electronics Conference},
    keywords = {Fiber lasers; Fluorescence lifetime imaging; Frequency doubled lasers; Laser sources; Live cell imaging; Master oscillator power amplifiers},
    pages = {ch_9_3},
    publisher = {Optical Society of America},
    title = {Sub-Nanosecond Pulsed Fiber Laser for 532nm Two-Photon Excitation Fluorescence (TPEF) Microscopy of UV transitions},
    year = {2019},
    keywords = {AG-Huber_NL},
    doi = { 10.1109/CLEOE-EQEC.2019.8872571},
    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 \[1\].},
    }