Multicolor flow cytometry - Understanding the basics [WEBINAR]

Find out more about Miltenyi Biotec's flow cytometry solutions: www.miltenyibi... Join Dr Guerric Epron and his webinar on the basics of flow cytometry, including fluorescence, compensation, data-spread effect, and panel design.
Explore more MACS Academy trainings and webinars: www.miltenyibi...
Miltenyi Biotec is a global provider of products and services that advance biomedical research and cellular therapy. Our innovative tools support research at every level, from basic research to translational research to clinical application. This integrated portfolio enables scientists and clinicians to obtain, analyze, and utilize the cell. Our technologies cover techniques of sample preparation, cell isolation, cell sorting, flow cytometry, cell culture, molecular analysis, and preclinical imaging. Our more than 25 years of expertise spans research areas including immunology, stem cell biology, neuroscience, and cancer, and clinical research areas like hematology, graft engineering, and apheresis. In our commitment to the scientific community, we also offer comprehensive scientific support, consultation, and expert training. Today, Miltenyi Biotec has more than 2,000 employees in 25 countries - all dedicated to helping researchers and clinicians around the world make a greater impact on science and health.

[@sahartahvili5081]

I've seen many tutorials and read many articles on Flow cytometry, you've made everything crystal clear. Miltenyi should be proud of having you.

[@pharmabaghdad]

I watched many videos about flow cytometry and this one is the best. Your way in explaining is much clearer than even flow cytometry articles! Thanks a lot. Please do more videos about flow cytometry.

[@prankrishnakakati1048]

You are a flow cytometry genius. A remarkable way of explanation. Please upload more videos on multicolour flow cytometry.

[@jamolabdo9939]

The best webinar I have ever watched. Thanks a lot!

[@frankfnl]

"Whenever you discuss compensation you'd better lock the door before when you start talking about this because people will just run away. They will try to escape" That part made my day.

[@Miltenyi_Biotec]

Glad you stayed in the room @Frank 😉

[@anestablished]

Trust me, you are not alone. Lessons learned......

[@rbkuwar]

This is very helpful to me. I'm new to the instrument. with this presentation, I am able to decipher some of the theoretical aspects of cytometer. Thank you for putting this.

[@karstenmiermans]

Excellent talk.

[@mohbashawat727]

an amazing presentation, I would like to ask for more presentations like this, your employer is lucky to have a brilliant scientist like you!

[@Biomeducated]

I had this exact training a while ago at my former company! Dr. Epron explained these concepts very clearly. I'm glad I found this on KZbin, good to recap the basic insights!

[@XamaL1]

Great explanation!

[@Seevawonderloaf]

Great seminar, thank you!

[@kf2606]

Fantastic!

[@alanxu3136]

Excellent !

[@qorazx]

Thank you so much for that extensive explanation. Really just what I needed

[@thurayae]

thank you so much! amazing explanation

[@Miltenyi_Biotec]

Glad you liked it!!

[@arvindpatel1166]

Great presentation as far as physics-related discussion.

[@CancerSleuth]

Best best best!!!

[@leilaaryan1575]

thanks a lot. This video is great help.

[@monkeymanolobaby]

So helpful, thank you!

[@ilianabarrera5505]

Brilliant presentation

[@gretelnusspaumer7233]

Thinking on write a good book on cytometry? Please go ahead!! State of art presentation. Liked a lot RAE Affinity.

[@yangxixiaoxue]

thank you.

[@alejandraordonez3187]

very nice!

[@curioussoul7338]

Really very helpful..

[@rangeo8783]

Can we apply two different lazers (e.g., FITC and PE) at the same time to excite cells, and then detect and sort only cells that are exicted by both lazers, and get data from computer? This would be the same effect by Image J. (e.g. Getting FITC and PE images, respectively from fluorescence microscope and then merge them, which generates yellow pseudo color)

[@Miltenyi_Biotec]

Hello range, depending on the capabilities of the flow cytometer, this is possible. Assuming your cells express antigens what can be bound through your PE and FITC labeled antibodies. If you really want to use two different lasers to sort the cells, you would need a cell sorter with a blue (to excite FITC) and a yellow (to excite PE) laser. After displaying your data with PE at one axe and FITC at the other in a so called “dot plot”, your PE pos, FITC pos cells would appear in the upper right corner and could be chosen for further cell sorting. If you just want to analyze and not to sort the cells with two different lasers, the MACSQuant® VYB is equipped with a blue and a yellow laser and would excite PE and FITC perfectly. But and this is important, if you just want to sort or analyze PE pos, FITC pos cells, it is not mandatory to use two different lasers. Both PE and FITC could also be excited with the blue laser alone but the signal would be detected through different detectors. Therefore the computer can still distinguish and sort the cells with our MACSQuant® Tyto® Cell Sorter for example.

[@SonaliSenguptasengupso41]

!!