Live Cell Imaging core facility
Live Cell Imaging core facility
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Live cell imaging 2025
This video was recorded by the Live Cell Imaging facility at the Karolinska Institute in Sweden during the LCI course 2024. It is intended as teaching material for microscopy users and facilities. Feel free to use it but please, mention the Live Cell imaging facility at KI, Sweden as the source of the video. You can also become a follower of our microscopy blog where we share tips and tricks about light microscopy (microscopykarolinska.se) or visit our website (ki.se/en/bionut/welcome-to-the-lci-facility).
Переглядів: 81

Відео

How to evaluate imaging efficiency and risk for bleedthrough- Part 1: Basic microscopy.
Переглядів 75Місяць тому
This video was recorded by the Live Cell Imaging facility at the Karolinska Institute in Sweden. It is intended as teaching material for microscopy users and facilities. Feel free to use it but please, mention the Live Cell Imaging core facility at Karolinska Institute in Sweden as the source of the video. You can also become a follower of our microscopy blog where we share tips and tricks abou...
How to create a tiled (large) image of a sample with unusual shape in NIS elements
Переглядів 593 місяці тому
This video was recorded by the Live Cell Imaging facility at the Karolinska Institute in Sweden during the LCI course 2024. It is intended as teaching material for microscopy users and facilities. Feel free to use it but please, mention the Live Cell imaging facility at KI, Sweden as the source of the video. You can also become a follower of our microscopy blog where we share tips and tricks ab...
How to acquire faster a tiled image with several colours and z-stack in NIS elements
Переглядів 503 місяці тому
This video was recorded by the Live Cell Imaging facility at the Karolinska Institute in Sweden during the LCI course 2024. It is intended as teaching material for microscopy users and facilities. Feel free to use it but please, mention the Live Cell imaging facility at KI, Sweden as the source of the video. You can also become a follower of our microscopy blog where we share tips and tricks ab...
How to use "Focus surface" function in NIS elements
Переглядів 1353 місяці тому
This video was recorded by the Live Cell Imaging facility at the Karolinska Institute in Sweden during the LCI course 2024. It is intended as teaching material for microscopy users and facilities. Feel free to use it but please, mention the Live Cell imaging facility at KI, Sweden as the source of the video. You can also become a follower of our microscopy blog where we share tips and tricks ab...
How to attach a coverslip to a microscope slide
Переглядів 1034 місяці тому
This video was recorded by the Live Cell Imaging facility at the Karolinska Institute in Sweden during the LCI course 2024. It is intended as teaching material for microscopy users and facilities. Feel free to use it but please, mention the Live Cell imaging facility at KI, Sweden as the source of the video. You can also become a follower of our microscopy blog where we share tips and tricks ab...
Removing coverslips from a 24 well plate
Переглядів 3474 місяці тому
This video was recorded by the Live Cell Imaging facility at the Karolinska Institute in Sweden during the LCI course 2024. It is intended as teaching material for microscopy users and facilities. Feel free to use it but please, mention the Live Cell imaging facility at KI, Sweden as the source of the video. You can also become a follower of our microscopy blog where we share tips and tricks ab...
Cleaning coverslips
Переглядів 3694 місяці тому
This video was recorded by the Live Cell Imaging facility at the Karolinska Institute in Sweden during the LCI course 2024. It is intended as teaching material for microscopy users and facilities. Feel free to use it but please, mention the Live Cell imaging facility at KI, Sweden as the source of the video. You can also become a follower of our microscopy blog where we share tips and tricks ab...
2024-02-15 - Introduction to Bioimage analysis
Переглядів 40310 місяців тому
This video was recorded by the Live Cell Imaging facility at the Karolinska Institute in Sweden during the LCI course 2024. It is intended as teaching material for microscopy users and facilities. Feel free to use it but please, mention the Live Cell imaging facility at KI, Sweden as the source of the video. You can also become a follower of our microscopy blog where we share tips and tricks ab...
2024 02 14 Ethics in imaging discussion part
Переглядів 3710 місяців тому
This video was recorded by the Live Cell Imaging facility at the Karolinska Institute in Sweden during the LCI course 2024. It is intended as teaching material for microscopy users and facilities. Feel free to use it but please, mention the Live Cell imaging facility at KI, Sweden as the source of the video. You can also become a follower of our microscopy blog where we share tips and tricks ab...
2024-02-14 - Ethics in imaging
Переглядів 6410 місяців тому
This video was recorded by the Live Cell Imaging facility at the Karolinska Institute in Sweden during the LCI course 2024. It is intended as teaching material for microscopy users and facilities. Feel free to use it but please, mention the Live Cell imaging facility at KI, Sweden as the source of the video. You can also become a follower of our microscopy blog where we share tips and tricks ab...
2024 02 14 Publishing images
Переглядів 10710 місяців тому
This video was recorded by the Live Cell Imaging facility at the Karolinska Institute in Sweden during the LCI course 2024. It is intended as teaching material for microscopy users and facilities. Feel free to use it but please, mention the Live Cell imaging facility at KI, Sweden as the source of the video. You can also become a follower of our microscopy blog where we share tips and tricks ab...
2024-02-14 - How to easily make figures for publication with OMERO figure
Переглядів 13010 місяців тому
This video was recorded by the Live Cell Imaging facility at the Karolinska Institute in Sweden during the LCI course 2024. It is intended as teaching material for microscopy users and facilities. Feel free to use it but please, mention the Live Cell imaging facility at KI, Sweden as the source of the video. You can also become a follower of our microscopy blog where we share tips and tricks ab...
2024-02-13 - Colocalization lecture and workshop
Переглядів 15410 місяців тому
This video was recorded by the Live Cell Imaging facility at the Karolinska Institute in Sweden during the LCI course 2024. It is intended as teaching material for microscopy users and facilities. Feel free to use it but please, mention the Live Cell imaging facility at KI, Sweden as the source of the video. You can also become a follower of our microscopy blog where we share tips and tricks ab...
2024 02 13 Artificial intelligence in microscopy images
Переглядів 10110 місяців тому
This video was recorded by the Live Cell Imaging facility at the Karolinska Institute in Sweden during the LCI course 2024. It is intended as teaching material for microscopy users and facilities. Feel free to use it but please, mention the Live Cell imaging facility at KI, Sweden as the source of the video. You can also become a follower of our microscopy blog where we share tips and tricks ab...
2024 02 13 Deconvolution workshop
Переглядів 7410 місяців тому
2024 02 13 Deconvolution workshop
2024-02-13 - Introduction to deconvolution
Переглядів 32510 місяців тому
2024-02-13 - Introduction to deconvolution
2024-02-13 - Introduction to super resolution microscopy
Переглядів 31510 місяців тому
2024-02-13 - Introduction to super resolution microscopy
2024-02-13 - High throughputcontent imaging
Переглядів 5810 місяців тому
2024-02-13 - High throughputcontent imaging
Camera Workshop 2024
Переглядів 8410 місяців тому
Camera Workshop 2024
2024 02 08 Saturation, underexposure, bit depth and image display aprt 2
Переглядів 9510 місяців тому
2024 02 08 Saturation, underexposure, bit depth and image display aprt 2
2024-0208 - Saturation, under exposure, bit depth, dynamic range and image display - part 1
Переглядів 13310 місяців тому
2024-0208 - Saturation, under exposure, bit depth, dynamic range and image display - part 1
Imaging multiple colours at once
Переглядів 11510 місяців тому
Imaging multiple colours at once
2024-02-07 - Signal, background and noise
Переглядів 14910 місяців тому
2024-02-07 - Signal, background and noise
2024-02-07 - Sensors
Переглядів 5910 місяців тому
2024-02-07 - Sensors
2024-02-07 - Bridging concepts Optical resolution contrast and sampling part 2
Переглядів 9610 місяців тому
2024-02-07 - Bridging concepts Optical resolution contrast and sampling part 2
2024-02-07 - Bridging concepts Optical resolution contrast and sampling - part 1
Переглядів 10110 місяців тому
2024-02-07 - Bridging concepts Optical resolution contrast and sampling - part 1
2024-02-06 Clearing and expansion microscopy
Переглядів 23610 місяців тому
2024-02-06 Clearing and expansion microscopy
Immunostaining troubleshooting
Переглядів 6810 місяців тому
Immunostaining troubleshooting
Sample preparation tips
Переглядів 18910 місяців тому
Sample preparation tips

КОМЕНТАРІ

  • @sivakumarjeyarajan3542
    @sivakumarjeyarajan3542 3 роки тому

    Hi Sylvie, Thanks for the wonderful tutorial. Wondering if the fluorescence for a cell or a region of cells can be monitored realtime with time?

  • @yahookossong8270
    @yahookossong8270 5 років тому

    Very useful video!

  • @gzclover
    @gzclover 5 років тому

    Thank you.

  • @dorianl.210
    @dorianl.210 5 років тому

    Hi Sylvie. I'm trying to generate points (center of objects) from the General Analysis in JOBS. I can detect the objects I want, but cant get the analysis to output point coordinates using the CentreX/Y in Features. How do I use the output from CentreX/Y, where can I retrieve the output? For example, I'd like create a point set based on detected objects and loop over the points after. Can you explain how to use General Analysis to generate point coordinates? you can also contact me at dorian.dleger@gmail.com THANKS!

    • @Livecellimagingfacility
      @Livecellimagingfacility 5 років тому

      Hi Dorian. In JOBS you need to create a Point list somewhere at the top of your pipeline (outside all loops). then in your general analysis in the channel where the objects are, you can point to the list. The position of each object will be saved there. This list can then be used to revisit the positions for e.g. new imaging with different settings. If you only want to save the positions and do not need to revisit them, all you need to do is select x and y under Save Binary/Object position in the channel where the objects are segmented. Good luck and happy new year! :)

  • @shaogonelee4481
    @shaogonelee4481 5 років тому

    very helpful

  • @irebustini
    @irebustini 6 років тому

    Excellent tutorial, very much needed in our lab. Thank you very much for sharing.

    • @Livecellimagingfacility
      @Livecellimagingfacility 6 років тому

      Thanks Ivan! Nice to know that our efforts are not in vain! Just above the videos on our website (ki.se/en/bionut/learning-microscopy), you can also download the Typical workflow of how to set a confocal. Our plan is to make a video explaining all this but it may help your lab in the meantime. :-) Sylvie

  • @ashadsaifi4140
    @ashadsaifi4140 6 років тому

    thanksss.

  • @moinulhoque2160
    @moinulhoque2160 6 років тому

    It's a nice video. Could you please make another video of how to do the coating?

    • @Livecellimagingfacility
      @Livecellimagingfacility 5 років тому

      Hi Moinul After cleaning and sterilizing the coverslips, simply put them on a piece of parafilm in a humid chamber (i.e. a box with paper soaked in water on the edges), add the solution you want to coat with, put a second coverslip on top so that you use the solution to coat 2 coverslips at the same time and you prevent evaporation on the edges. Close the humid chamber during incubation time (which is often at room temperature but it depends on what you are coating). When the coating is done, carefully remove the top coverslip, flip it so that the coated side is upwards, remove the solution (often can be stored and reused) from the bottom coverslip. Rinse all coverslips with PBS. They are ready to be used. Make sure you keep track of which side was coated. Good luck!

    • @janggeumseo592
      @janggeumseo592 3 роки тому

      @@Livecellimagingfacility Hello, I am trying to coat 13mm round coverslips with collagen. But I am very new to this area. I tried to add 10-20 microliter collagen solution on top of coverslips but it was very hard to spread them uniformly with pipette tip. Dipping them in solution is not useful because both sides will be coated. In the method you explained; second coverslip is put on top of first coverslip and they are located in the solution so outer surfaces will be coated whilst inner surfaces will remain uncoated. This is my understanding. could you please help me with that? I also don't have humid chamber and never used it before. Thank you!

    • @Livecellimagingfacility
      @Livecellimagingfacility 3 роки тому

      sorry for not answering earlier. Somehow I did not get notified of your comment. Yes you are totally correct in your understanding. We sandwich the coating solution between 2 coverslips so only 1 side of the coverslip gets coated. To make a humid chamber, simply take a Petri dish, put a piece of parafilm completely flat at the bottom, place some absorbant paper at the periphery of the dish and wet them completely but not enough for the water to run out. There you have a cheap and simple humid chamber! :)

  • @Mgrati
    @Mgrati 7 років тому

    Very Helpful! Thanks!

  • @taregomer7376
    @taregomer7376 7 років тому

    Thanks for the excellent tutorial. A similar one on acquiring time lapse images would be greatly helpful.

    • @Livecellimagingfacility
      @Livecellimagingfacility 7 років тому

      very happy you found it useful Tareg. for timelapse, it is super simple. set all your imaging parameters so that you get the type of images you want then set your time interval and repeats in the ND acquisition tab under the time tab. then press run now. :)