Running a Basic 2 color Flow Cytometry Experiment in BD FACS Diva

  Рет қаралды 142,321

UC Merced SCIF Stem Cell Instrumentation Foundry

UC Merced SCIF Stem Cell Instrumentation Foundry

Күн бұрын

Пікірлер: 84
@laxmanegalitarian8581
@laxmanegalitarian8581 6 ай бұрын
Man, you deserve to earn $150 for every full video watched. I literally took a 2 hours training on Flow Cytometry yesterday ($75 an hour, paid by the lab though) from some super speed instructor who would not wait for me to take notes even and learned literally nothing. As soon as you started explaining what all those windows were, I knew your video is going to be great. This must be the most beautifully explained video for flow cytometry on the internet. Thank you man, I wasted my lab's money yesterday and I am learning from you today. I will watch your next video on compensation too.
@a.a.2277
@a.a.2277 6 жыл бұрын
This was the clearest explanation I ever get about FACS and flow. It helped me a lot to understand. Thank you very much!
@Biomeducated
@Biomeducated 5 жыл бұрын
Most interestingly it's a good showcase on how to use FACS Diva software! Sooooo helpful!
@DrShafi-xn6pk
@DrShafi-xn6pk 4 ай бұрын
This is so far the best video I have seen on FACS DIVA to set an experiment, to set controls, and to resolve different populations
@juanr859
@juanr859 Жыл бұрын
Excellent presentation. It is clear, concise and engaging. I truly appreciate your willingness to share your expertise.
@dotheneedful55
@dotheneedful55 10 ай бұрын
Thank you soo very much! I have been searching forba clear cut explanation that isnt just someone explaining the theory.
@yuantian5320
@yuantian5320 4 жыл бұрын
this tutorial is much better than the previous training I received, even that trainer speaks my native language and you explain all in English.
@jazmincastro9248
@jazmincastro9248 3 ай бұрын
I can't say enough, THANK YOU SO VERY MUCH for this!!!!! FANTASTIC video and explanation
@prakritikarki3740
@prakritikarki3740 Жыл бұрын
The best video for flow cytometry experiment found ever
@sanmaybanerjee
@sanmaybanerjee 5 жыл бұрын
This is a mind-blowingly good demonstration. Seriously, mate. Thanks a lot.
@lillianliu2084
@lillianliu2084 4 ай бұрын
Very nice video and clearly explained the basic operation of FACSDiva. Though I got trained by our core facility, your video made me less frustrated for learning to use this complex machine and software.
@ChakravarthyGarlapati
@ChakravarthyGarlapati 3 жыл бұрын
Dude I thought of making one of these videos as so many of my friends are asking. You explained it nicely. I can simply share your video if someone asks. By the way you have nicely done it covering each and every point needed for the beginners.
@tpankajavalli
@tpankajavalli Жыл бұрын
Excellent demo! Extremely helpful, thanks for sharing this video!
@preston1382
@preston1382 Жыл бұрын
Thank you for being much more helpful than anyone in my lab or institution. Much appreciated 🙏
@jackwining1928
@jackwining1928 2 жыл бұрын
Lovely presentation for the flow cytometry. It really helped me a lot. Many thanks.
@shameera4811
@shameera4811 7 жыл бұрын
Great demonstration!!! Thank you very much for the upload.
@nadeekabandara5504
@nadeekabandara5504 6 жыл бұрын
This is an excellent demonstration
@mariakalomoiri7403
@mariakalomoiri7403 3 жыл бұрын
Amazing demonstration of FACS Diva! Thank you so much for this helpful video!
@โสฐิดากาเหย็ม
@โสฐิดากาเหย็ม 7 ай бұрын
thank you so much for good demonstration!!! Extremely helpful!!!
@VGliffe
@VGliffe 6 жыл бұрын
Thank you very much for the video. It definitely helped to backup what I learned. Would love to see one with compensation.
@siavashmashhouri4969
@siavashmashhouri4969 5 жыл бұрын
Great, better than our technicians :). Thanks
@xinyiwang2956
@xinyiwang2956 2 жыл бұрын
Thank you!!! That makes sense for the beginner!
@kimle7049
@kimle7049 2 жыл бұрын
Thank you for such a great video! I am learning flow cytometry and this helps a lot
@alexandroskourtesakis3673
@alexandroskourtesakis3673 4 жыл бұрын
Very good demonstration! Extremely helpful!
@sabrarostami4465
@sabrarostami4465 3 жыл бұрын
Thank you very much, this is really enlightening.
@TotodileDragon
@TotodileDragon 5 жыл бұрын
This is a great compensation tutorial, amazing work! I wish I would have found this sooner :'c
@lusen5917
@lusen5917 4 жыл бұрын
clearest explanation!excellent job! thank you very much。
@nabilahbaby6242
@nabilahbaby6242 2 жыл бұрын
Thanks a lot! Very clearly explained...
@karthikeyanbio
@karthikeyanbio 2 жыл бұрын
Thanks bro. This really helped a lot.
@lix4793
@lix4793 5 жыл бұрын
very helpful! Indeed today I just wondered how to adjust the voltage and how to set up p2/p3/p4. Thanks a lot!
@mermerrrrrrrrr
@mermerrrrrrrrr 9 ай бұрын
very well explained...thank you so much
@ardy4444
@ardy4444 3 жыл бұрын
Very useful and clearly explained.
@vincenthuang6341
@vincenthuang6341 5 жыл бұрын
Thank you VERY MUCH! Very hopeful! Please keep up the good work!
@sAyWaHhFuL
@sAyWaHhFuL 6 жыл бұрын
Yasss, you did it with this explanation! Thanks a lot!!
@faborodeo.samuel5913
@faborodeo.samuel5913 5 жыл бұрын
This is fantastic work. Thank you for sharing.
@amrishsharma457
@amrishsharma457 3 жыл бұрын
The best tutorial of voltage setting.Wish there were more than 2 colors though. How do you set voltage for like 3 colors. For instance, say you have PE, PerCPcy5.5 and FITC. Would you then look for setting voltage with FITC against PE and PerCPcy5.5?
@josephkamtchumtatuene521
@josephkamtchumtatuene521 5 жыл бұрын
Excellent video. Thank you very much! I am a beginner with Flow Cytometry and have been struggling to find someone to give clear step-by-step explanations. Question: Is there a minimum number of cells per tube that you would recommend in order to have a good experiment? Thanks!
@khalidrashid2684
@khalidrashid2684 4 жыл бұрын
Fantastic video. Thanks
@kavitavats3581
@kavitavats3581 5 жыл бұрын
very easy explanation.Good video
@elhamshamsaei1946
@elhamshamsaei1946 3 жыл бұрын
Many thanks this was great
@same2100
@same2100 4 жыл бұрын
Thanks a lot, I learnt lots of useful things.
@Biomeducated
@Biomeducated 5 жыл бұрын
You are a life saver! Thanks!
@perikalaa
@perikalaa 5 жыл бұрын
Great Demonstration would you please add more videos on FACS and other cytometers
@hongxiachen778
@hongxiachen778 Жыл бұрын
😀Very useful. Thanks,
@nesrinyasseralissa1735
@nesrinyasseralissa1735 4 жыл бұрын
Great demonstration, thank youu
@sohanaaktermina7057
@sohanaaktermina7057 Жыл бұрын
Clear explannation
@preetibhadauria4315
@preetibhadauria4315 6 жыл бұрын
Very well explained. Thanks for the detailed information.
@roove1537
@roove1537 3 жыл бұрын
Thank you for this!
@shijie3224
@shijie3224 5 жыл бұрын
It really helps. Thank you very much!!
@danielryan855
@danielryan855 6 жыл бұрын
Very clear video with great detail. Do you have a video of the setup of a more complex experiment? One that would require compensation.
@sintayehufekadu5979
@sintayehufekadu5979 6 жыл бұрын
Thank you very much. It was very understandable video.
@daliatarantino6781
@daliatarantino6781 4 жыл бұрын
thank you so much, this is really helpful!
@jingzhao9300
@jingzhao9300 6 жыл бұрын
This is really helpful! Thank you soooo much!!
@hba3820
@hba3820 5 жыл бұрын
Thank you very much! that helpes a lot
@shimaashehata4233
@shimaashehata4233 6 жыл бұрын
Thank you so much for this video. I learned from it a lot. This is the best video so far explaining the basics of how to run samples with 2 flourophores. I am a beginner in flow cytometry and I got a lot of info from this video. I have a question, I found that some people do a dot plot for FSC-A Vs FSC-H dot plot, is this plot gives the same info as FSC Vs SC dot plot regarding giving info about doublet and singlet cells?
@Biomeducated
@Biomeducated 5 жыл бұрын
No, those are 2 separate plots. You start with FSC vs SSC to eliminate debris (usually below the 50K markers on both axes somewhere. Next is to draw FSC-A (X) vs FSC-H (Y): the singlets are all on the diagonal. The doublets stick out to the right on the X-axis and should not be included in your gate. You can set the same for SSC (SSC-A vs SSC-H). Some people use these consecutively to eliminate doublets both according to FSC, and subsequently according to SSC. Cheers!
@prof1400
@prof1400 6 жыл бұрын
Very helpful. Thank you very much.
@M_Alatawi
@M_Alatawi 2 жыл бұрын
Many Thanks
@aragawgebeyehu8304
@aragawgebeyehu8304 Жыл бұрын
Thank you!!!!!
@gus.f762
@gus.f762 4 жыл бұрын
Great job, thank you!!!!
@victornegri7763
@victornegri7763 6 жыл бұрын
Very helpful! Thank you
@tillyfreeman5192
@tillyfreeman5192 2 жыл бұрын
Where do we get the user manual for this instrument?
@caomoyulong
@caomoyulong 7 жыл бұрын
Very helpful! Thanks!!
@arasharjomand7970
@arasharjomand7970 6 жыл бұрын
Great work,, cheers
@issamel9036
@issamel9036 7 жыл бұрын
Thankyou. This was super helpful ;)
@ahussbinwali
@ahussbinwali 7 жыл бұрын
Thanks a lot,. very helpful!
@reallegend1
@reallegend1 7 жыл бұрын
so nice explanation , thanks
@tillyfreeman5192
@tillyfreeman5192 2 жыл бұрын
Hi, may I know the name and background of the presenter? Thank you. This video is so valuable!
@ruihuama8157
@ruihuama8157 5 жыл бұрын
Thank you, very helpful
@samarjitmaharana3484
@samarjitmaharana3484 6 жыл бұрын
I have one doubt. Is it needed to link the experiment to any of lysed wash or lysed no wash parameters everytime when ever you are doing compensation with single tubes each colour.
@Dezzy7model
@Dezzy7model 6 жыл бұрын
This was helpful. Thanks a lot :)
@edileneoliveira991
@edileneoliveira991 6 жыл бұрын
Great! Thank you!
@monspark2317
@monspark2317 7 жыл бұрын
Thank you
@jyotsnakhithani2241
@jyotsnakhithani2241 5 жыл бұрын
Thank you so much
@kimle7049
@kimle7049 2 жыл бұрын
When you ran the compensation, did you run Low or High? And also for the cells? Thanks
@hedgefield
@hedgefield 6 жыл бұрын
THANK YOU
@justojosecortesquijano1274
@justojosecortesquijano1274 4 жыл бұрын
con conocimiento TECNOLOGÍA CONSTRUCCIÓN en el proceso constructivo en la resoluciones de NRS 2010
@redtails
@redtails 3 жыл бұрын
My institution offers a 2 hour tutorial for what you're showing in half an hour here
@justojosecortesquijano1274
@justojosecortesquijano1274 4 жыл бұрын
justo jose cortes quijano tecnología construcción ingresado del sena con tarjeta del copnia
@SajadAhmad-bi1fp
@SajadAhmad-bi1fp 2 жыл бұрын
video quality is extremely poor so sad
@Sama-sf4sy
@Sama-sf4sy 2 жыл бұрын
Thank you so much. It's very useful!
@सविन-झ4झ
@सविन-झ4झ 3 жыл бұрын
Thank you so much
@mkaiyu
@mkaiyu 6 жыл бұрын
Very helpful! Thanks so much!
Compensation of a 7 color panel on the BD LSR II
21:43
UC Merced SCIF Stem Cell Instrumentation Foundry
Рет қаралды 106 М.
BD FACS Aria startup procedure UC Merced
30:28
UC Merced SCIF Stem Cell Instrumentation Foundry
Рет қаралды 32 М.
We Attempted The Impossible 😱
00:54
Topper Guild
Рет қаралды 56 МЛН
Quilt Challenge, No Skills, Just Luck#Funnyfamily #Partygames #Funny
00:32
Family Games Media
Рет қаралды 55 МЛН
The Best Band 😅 #toshleh #viralshort
00:11
Toshleh
Рет қаралды 22 МЛН
OpenFlow: Introduction to Flow Cytometric Data Analysis Part I
1:33:26
OpenFlow Cytometry
Рет қаралды 41 М.
Multicolor flow cytometry - Understanding the basics [WEBINAR]
51:22
Miltenyi Biotec
Рет қаралды 77 М.
Flow Basics 2.1: The Basic Staining Protocol
25:39
UChicago Flow
Рет қаралды 24 М.
CAT Hands-On Training: The DIVA Software
34:23
UChicago Flow
Рет қаралды 11 М.
Lecture 7b: Flow Cytometry
34:10
Annelise Snyder
Рет қаралды 36 М.
BD Fortessa X-20 -Setting Up an Experiment in DIVA software
31:16
Flow Cytometry And Cell Sorting Facility-TAMU HSC
Рет қаралды 1,9 М.
Flow Cytometry & FACS  |  Beginner Data Interpretation Tutorial
8:42
The Principle of Flow Cytometry and FACS (2- FACS: Fluorescence Activated Cell Sorting)
17:40
Biomedical and Biological Sciences
Рет қаралды 128 М.
Tutorial on tSNE and FlowSOM Step-by-Step tool usage in FlowJo V10
1:21:20
UC Merced SCIF Stem Cell Instrumentation Foundry
Рет қаралды 35 М.
We Attempted The Impossible 😱
00:54
Topper Guild
Рет қаралды 56 МЛН