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The microscope was coupled to a camera-type Axiocam HRC color Carl Zeis technology, operating with Axiovision logiciel version 3.1.
The microscope was coupled with a tunneling current detection, in order to study the interactions between the sample and the probe during scanning.
A light microscope was coupled to the flat sheet die of a laboratory extruder allowing on-line morphology measurements during the extrusion of polymer blends.
The microscope was coupled to a black-and-white camera (DS-Qi1Mc; Nikon) operated by the Nikon Elements AR3.0 software (NES AR3.0) for image acquisitions.
The microscope was coupled to a black-and-white camera (DS-Qi1Mc; Nikon) operated by the Nikon Elements AR3.0 software (NES AR3.0).
The microscope was coupled to the FastFLIM frequency domain system (ISS, Champaign, IL) and uses a 0.5 mW 448 nm diode laser modulated at a fundamental frequency of 20 MHz for excitation of mCerulean.
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This microscope is coupled to an EM-CCD camera (Luca-S, Andor™, Ireland).
Two fluorescence microscopes were coupled to a synchrotron beam for excitation at 275 nm.
The FCS system was built around a FV300 Olympus laser scanning confocal microscope, where an additional FCS module was coupled to the microscope.
Study Design and Setting: A CO2 laser and operating microscope (400-mm focal length) was coupled to either a reflective (Cassegrain-like) or refractive micromanipulator.
The microscopic views were binarised and automatically recognised using Luzex AP software (Nireco, Tokyo, Japan) that was coupled to the microscope via a CCD video camera.
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