In vivo fluorescence microscopy via iterative multi-photon adaptive compensation technique
نویسندگان
چکیده
منابع مشابه
Adaptive optics two-photon fluorescence microscopy
Non-linear imaging is widely used in biological imaging, primarily because of its ability to image through tissue to depth of a few hundred micrometers. Because two photons need to be absorbed to excite a fluorophore in this instrument, the probability of fluorescence emission of a detectable photon scales with the intensity squared of the beam. As a result, aberrations in the beam path that re...
متن کاملAdaptive optics two photon scanning laser fluorescence microscopy
Two-photon fluorescence microscopy provides a powerful tool for deep tissue imaging. However, optical aberrations from illumination beam path limit imaging depth and resolution. Adaptive Optics (AO) is found to be useful to compensate for optical aberrations and improve image resolution and contrast from two-photon excitation. We have developed an AO system relying on a MEMS Deformable Mirror (...
متن کاملTwo-photon Fluorescence Light Microscopy
The invention of two-photon fluorescence light microscopy by Denk, Webb and co-workers (Denk et al., 1990) revolutionized three-dimensional (3D) in vivo imaging of cells and tissues. In 1931, the theoretical basis of twophoton excitation was established by Maria GöppertMayer, and this photophysical effect was verified experimentally by Kaiser and Garret in 1963. Two-photon excitation is a fluor...
متن کاملTwo-photon excitation fluorescence microscopy.
Two-photon fluorescence microscopy is one of the most important recent inventions in biological imaging. This technology enables noninvasive study of biological specimens in three dimensions with submicrometer resolution. Two-photon excitation of fluorophores results from the simultaneous absorption of two photons. This excitation process has a number of unique advantages, such as reduced speci...
متن کاملThree-photon excitation in fluorescence microscopy.
We show experiments proving the feasibility of scanning fluorescence microscopy by three-photon excitation. Three-photon excitation fluorescence axial images are shown of polystyrene beads stained with the fluorophore 2,5-bis(4-biphenyl)oxazole (BBO). Three-photon excitation is performed at an excitation wavelength of 900 nm and with pulses of 130 fs duration provided by a mode-locked titanium-...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: Optics Express
سال: 2014
ISSN: 1094-4087
DOI: 10.1364/oe.22.023786