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Multiphoton Publications

  • An Evaluation of Two-Photon Excitation Versus Confocal and Digital Deconvolution Fluoescence Microscopy Imaging in Xenopus Morphogenesis
    Microscopy Research and Technique 47:172-181 (1999)
  • Journal (JBO) Special Section on MP
    Journal of Biomedical Optics,July 2003
  • Characterization of Two-photon Excitation Fluorescence Lifetime Imaging Microscopy for Protein Localization
    MICROSCOPY RESEARCH AND TECHNIQUE 63:72–80 (2004)

  • An Evaluation of Two-Photon Excitation Versus Confocal and Digital Deconvolution Fluoescence Microscopy Imaging in Xenopus Morphogenesis
    by Ammasi Periasamy

    ABSTRACT: The ability to visualize cell motility occurring deep in the context of opaque tissues will allow many currently intractable issues in developmental biology and organogenesis to be addressed. In this study, we compare two-photon excitation with laser scanning confocal and conventional digital deconvolution fluorescence microscopy, using the same optical configuration, for their ability to resolve cell shape deep in Xenopus gastrula and neurula tissues....
    Microscopy Research and Technique 47:172-181 (1999)
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    Journal (JBO) Special Section on MP
    by Ammasi Periasamy, Ph.D. Alberto Diaspro, Ph.D.
    Introduction   Table of Contents   Top


    Characterization of Two-photon Excitation Fluorescence Lifetime Imaging Microscopy for Protein Localization
    YE CHEN AND AMMASI PERIASAMY

    ABSTRACT Two-photon excitation .uorescence resonance energy transfer (2P-FRET) imaging microscopy can provide details of speci.c protein molecule interactions inside living cells. Fluorophore molecules used for 2P-FRET imaging have characteristic absorption and emission spectra that introduce spectral cross-talk (bleed-through) in the FRET signal that should be removed in the 2P-FRET images, to establish that ........
    MICROSCOPY RESEARCH AND TECHNIQUE 63:72–80 (2004)
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