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In Vivo Three-Dimensional Two-Photon Microscopy to Study Conducted Vascular Responses by Local ATP Ejection Using a Glass Micro-Pipette
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Confocal & Two-photon Microscopy - SlideServe
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In this video you can see RPE1 cells transfected with H2B-GFP plasmid (maximum intensity projection of 117 z planes). Courtesy of Tingsheng Liu, Mitosis Lab, Singapore. It shows the difference between LSM and the new LSM Plus processing. LSM Plus is a new linear Wiener filter deconvolution, that needs next to no interaction while still ensuring a reliable quantitative result. Regardless of whether you perform classic confocal or advanced multispectral imaging including NLO and NIR. Just as in th
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In this video you can see RPE1 cells transfected with H2B-GFP plasmi…
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Graphene Liquid Cell Electron Microscopy | JoVE Journal
Graphene Liquid Cell Electron Microscopy | JoVE Journal
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Two-photon excitation microscopy: Why two is better than one
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