Fluorescence images were collected using Axioplan2 imaging microscope and a Sensicam 12BIT camera (Zeiss, Jena, Germany).
Images were taken using a Zeiss Axioplan-2 imaging microscope with the digital image-processing program AxioVision 4.3 (Zeiss, Jena, Germany).
Sections were analyzed using a Zeiss Axioplan-2 imaging microscope with the scientific image processing software AxioVision 4.6 (Zeiss, Jena, Germany).
Raman spectra were conducted with Ar-ion laser of 532 nm using the Via Reflex Raman imaging microscope system.
For the micro-FTIR measurement, a Perkin-Elmer Spotlight 200 infrared imaging microscope interfaced to a Spectrum One Fourier transform infrared spectrophotometer (Perkin Elmer) was used.
The resulting arrays were imaged by a hyperspectral imaging microscope.
The new DXR2xi Raman imaging microscope is image-centric and works much like the scanning microscopes already used by many scientists.
The samples were imaged using a ZEISS Axioplan2 imaging microscope (Carl Zeiss, Germany).
The neurons were imaged with an Axioplan 2 imaging microscope (Zeiss, Germany) equipped with an ApoTome module (Zeiss, Germany).
Stained cells were imaged using a Zeiss Axioplan 2 imaging microscope with a 100× Plan-Apochromat 1.40 oil objective at room temperature.
Specimens were analyzed with a Zeiss Axioplan-2 imaging microscope and the digital image-processing program AxioVision 4.6 (Zeiss, Jena, Germany).
