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MULTIPHOTON MICROSCOPY: Turnkey femtosecond lasers fuel growth of multiphoton imaging

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MULTIPHOTON MICROSCOPY: Turnkey femtosecond lasers fuel growth of multiphoton imaging

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  • Author: Arnd Krueger
In conventional confocal laser scanning microscopy, the fluorescence excitation source is a tightly focused continuouswave (CW) laser beam. The laser beam waist is re-imaged onto a pinhole (the confocal aperture), which prevents fluorescence generated outside the focal plane from reaching the detector.

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