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This system synchronizes laser light stimulation and imaging with 2 independent IR lasers for multiphoton imaging. Laser light stimulation is done with a multiphoton laser, allowing pinpoint stimulation of areas deep within a specimen that cannot be reached with single photon. Multiphoton stimulation can be done at a pinpoint, allowing observation of the effect a single dendritic spine has. Laser light stimulation can be performed in 3 dimensions or locally at specific sites.

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This system is equipped with an IR laser in the scanner for stimulation. In addition to general multiphoton microscopy, the system allows pinpoint light stimulation by multiphoton excitation during imaging with a visible laser.
Multiphoton microscopy does not allow some image acquisition modes such as Time Controller.

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This system is equipped with an IR laser for multiphoton imaging and laser for visible light, so it is designed for deep imaging by multiphoton microscopy and confocal imaging with a visible laser. The system is designed for varied imaging including Live Cell and in vivo imaging.
Using this system along with the double laser combiner allows multiphoton imaging and visible light stimulation.
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This dedicated multiphoton system is not equipped with a visble light laser. Simple optics optimized for multiphoton microscopy allow a smaller size, simple operation, and imaging deep within the sample. The system uses a gold-coated galvanometer scanning mirror.
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The femtoCARS add-on unit shares a standard femtosecond laser with FV1000MPE. It is a separate unit that can be added to most FV1000MPE configurations. The add-on unit is designed to image molecules rich in lipid (CH2) using Coherent Anti-Stokes Raman Scattering (CARS) microscopy.
The femtoCARS add-on unit is only available in US and Canada currently.

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* The use of lasers with a SUB-PICOSECOND pulse for two-photon microscopy is protected by U.S. and Canada Patent No. 5,034,613. This technology was integrated in Olympus laser scanning microscopy, Model FV1000MPE, under a license from Carl Zeiss MicroImaging GmbH and Cornell Research Foundation Inc.
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