Introduction to Light Sheet Microscopy

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  • Опубликовано: 3 июл 2024
  • In this presentation, we will review the current state and challenges of conventional microscopy and the goals for light sheet microscopy. See an in-depth overview of various techniques associated with Light Sheet, and how to successfully overcome specific demands that are inherent with imaging physiological processes.
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Комментарии • 12

  • @AZ-qx1xd
    @AZ-qx1xd 3 года назад +7

    This is so thoroughly explained. Thank you very much!

  • @spicesmiles
    @spicesmiles Год назад

    goodness! thank you
    Agreed, thorough and clearly explained❣
    I really like your including comparisons of other microscopy techniques helps us understand how combining multiple microscopy capabilities can aid in achieving ideal testing. phenomenal!

  • @gabrielchatelain9106
    @gabrielchatelain9106 Год назад

    Amazingly clear talk! Thank you so much

  • @dimitrispapageorgiou2711
    @dimitrispapageorgiou2711 Год назад

    That's a great video on the topic! Thank you for this thorough presentation.

  • @Mathias-qs9vn
    @Mathias-qs9vn 3 года назад

    men for real thank you make me feel better on this subject !

  • @jonnathansingh3705
    @jonnathansingh3705 Год назад

    Amazing - thanks a lot for this resource, super clearly explained, useful, and kind of you to upload this for free.

  • @beautifulmusic2551
    @beautifulmusic2551 3 года назад

    Great cover. Appreciate!

  • @RossOCarroll3301
    @RossOCarroll3301 2 года назад

    Amazing thank you!

  • @yihansong6338
    @yihansong6338 3 года назад

    Thx, it helps a lot

  • @danish07delhi
    @danish07delhi 2 года назад

    Thanks a lot!

  • @stacka9736
    @stacka9736 Год назад

    hello, why the LSFM is diffraction limited and on wikipedia in french there is write that Sidentopf and Zigmondy manage to pass the diffraction barrier with the ultra microscope

  • @lotharmayring6063
    @lotharmayring6063 6 месяцев назад

    making light sheets is not nessesary because the objectiv and foto stacking have this possibility and fluorescenc-microscopy still gives unsharp images. Light sheets are still thicker than tocal plane sharpness. Here much theory is given but i see no results