Fluorescence Filters: Imaging Multiple Fluorophores & Dealing with Bleed-through

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  • Опубликовано: 3 июл 2024
  • *This video walks you through best practices for imaging more than one fluorophore, including critical controls experiments, why bleed-through can occur when imaging multiple fluorophores and various strategies for reducing bleed-through. Enjoy!
    * Visit FPbase.org/microscopes to generate a custom spectraviewer for your microscope.
    * Visit Image.sc for expert help with calculating bleedthrough coefficient and image arithmetic.
    * Visit Forum.microlist.org for expert help on the microscopy and sample preparation methods discussed in this Microcourse.
    * Jost & Waters, 2019: doi.org/10.1083/jcb.201812109
    * French subtitles were provided by BioImaging North America.
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Комментарии • 7

  • @conehenge77
    @conehenge77 2 месяца назад

    Thank you so much!! That was very helpful.

  • @woongyoungso4838
    @woongyoungso4838 4 года назад +5

    Thanks for the awesome content! Looking forward to more!

  • @jessebrunsveld1
    @jessebrunsveld1 4 года назад +1

    Great channel and explanation, thanks!

  • @Walaa918
    @Walaa918 4 года назад

    Very helpful

  • @hosseinghasemi1659
    @hosseinghasemi1659 7 месяцев назад

    awesome

  • @rachanasomaiya8032
    @rachanasomaiya8032 4 года назад

    Thank you!!!!

  • @lotharmayring6063
    @lotharmayring6063 Месяц назад

    that is not the prolem of FM. The problem is that the images ar so unsharp. DIC is much better