Microscopy: Introduction to Fluorescence Microscopy (Nico Stuurman)

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iBiology Techniques

iBiology Techniques

Күн бұрын

Пікірлер: 93
@carposporophyte
@carposporophyte 5 жыл бұрын
You can see in his eyes all the time he has dedicated in his life to this subject he loves so much.
@sschw006
@sschw006 10 жыл бұрын
could not of asked for a better, well presented explanation of fluorescence. Very nicely done.
@poetryodia6704
@poetryodia6704 3 жыл бұрын
Thank you so much..no one has explained as good as you. Thank you iBiology🙏
@tessahemrika7150
@tessahemrika7150 10 жыл бұрын
Thank you so much for this presentation, for the very first time I actually get it!
@exodusofficer
@exodusofficer Жыл бұрын
Thank you! I am a researcher who works with polarizing microscopes and I am trying to get into fluorescence work. Out of a dozen video lectures on the topic, several textbook chapters, and a pile of research papers, this video is the first time that most of this has made sense. I especially appreciate the detailed description of the filters, most lectures leave a LOT out on those. I still have some advanced questions about the light source, and how UV fits into this (is it also produced by the Hg lamp?), but I finally feel that I am making progress on this!
@harykappiri8091
@harykappiri8091 Жыл бұрын
Thank you for the Lecture Sir,very detailed, I have been working in Diamonds since 1998, I have to study more in Fluorescence of Diamonds, Please provide if you have any information ,
@naturephile554
@naturephile554 3 жыл бұрын
Your way of explanation by using tools is really aid in learning....thank you for making such nice and helpful video !!!!
@elleoops777
@elleoops777 9 жыл бұрын
Excellent video, would be nice to see a tutorial on specimens preparation and various staining techniques. I have found specimen preparation and technique is more important than the mechanical understanding of the process. I am sure your techniques would be another excellent tutorial from you! Thanks
@은우성
@은우성 3 жыл бұрын
im korean, and i'd appreciate this video that is so intutive and well explained
@MrSharkboy6
@MrSharkboy6 7 күн бұрын
This was so awesome. Made it a joy to learn about.
@BioPhys92
@BioPhys92 Жыл бұрын
It's a very complicated subject, and you are doing a good job here. Thanks
@mervatel-deftar8412
@mervatel-deftar8412 5 жыл бұрын
Amazing lecture very simplified but of high level. thank you very much it was very helpful.
@rnd9331
@rnd9331 6 жыл бұрын
haha play 32:19, he says fkd up instead of fluorescent :P Great lecture btw
@funyi3
@funyi3 6 жыл бұрын
there should be some beeep sound
@neoretrodude
@neoretrodude 4 жыл бұрын
I went straight to it
@khadijaw1630
@khadijaw1630 3 жыл бұрын
i am so impressed how did you even notice that:) great attention, love that for you
@annmaryjoseph6147
@annmaryjoseph6147 2 жыл бұрын
Such a wonderful, in detail presentation. Thank you Sir
@sebastian5671
@sebastian5671 2 жыл бұрын
I have my first course in nanoengineering, this really helped, thanks a lot!
@Gealamusic
@Gealamusic 2 жыл бұрын
thank you so much - really helped me get into my term paper about fluorescence microscopy
@goodluckdominique7255
@goodluckdominique7255 5 жыл бұрын
This video help me a lot, I use alpha-tubiline antibody, a lot of time to see, reveal microtubules in the cell, but the image (spindle) was not clear, after watching these videos, I did and it works. Thank you.
@hitsong-cutegirl
@hitsong-cutegirl Жыл бұрын
Thank you for knowledge. 😊❤
@DaruoshAghajaney
@DaruoshAghajaney 5 жыл бұрын
Excellent lecture and demonstration. Really impressive.
@drichhapurak
@drichhapurak 6 жыл бұрын
very well explained,video makes clear the principle and working of Fluorescence microscopy,thanks
@DMOND-qg2cg
@DMOND-qg2cg 3 жыл бұрын
frodo teaching me biology, gotta love it
@stephensonal4082
@stephensonal4082 3 жыл бұрын
Great, clear, and informative presentation. Thank you
@evanescent1000
@evanescent1000 6 жыл бұрын
Thank you for this helpful introduction. I believe the quantum efficiency (QE) explained in this video is more commonly referred to as quantum yield. QE is a term used for the camera or detector that is capturing the photons.
@haoguo2056
@haoguo2056 10 жыл бұрын
Good job. This is a very thorough lecture.
@nellyflorestapia
@nellyflorestapia 11 жыл бұрын
Great job, well explained, thak you for everything
@etiennecartier1
@etiennecartier1 10 жыл бұрын
love it! At last I understand how those "cubes" really work!
@ulisesmontero950
@ulisesmontero950 4 жыл бұрын
Hello, excellent video, I need help, I would like to know which ones, with the advantages and disadvantages of fluorescence, sorry if you do not understand the question well, I speak Spanish.
@mr702s
@mr702s 4 жыл бұрын
Is there a microscope which allows to collect all these types of exposures at once for a detailed (colored) video compilation of samples in motion? Rather than via a turret limited to one exposure at a time?
@zhang_han
@zhang_han 3 жыл бұрын
12:00 I'm a bit confused by the diagram. Is S0,0 and S0,2 the same energy or is S0,2 higher? Because it looks like there's a photon of the same wavelength being emitted when an electron drops from S1 to S0,0 and S0,2 but that can't be if they're different energy levels, right?
@seaweedseaside5905
@seaweedseaside5905 6 жыл бұрын
Thank you for the clear and thorough presentation. Is fluorescence microscopy in general really quantitative, though? The local environment of the fluorophore can have an effect on the fluorescence quantum yield and the fluorescence spectrum of the fluorophore, making it difficult to draw a direct correlation between fluorescence intensity and fluorophore concentration. Am I right? I guess this problem can be circumvented by using fluorescence lifetime imaging microscopy, in which the information (i.e., the fluorescence lifetime at each pixel) is independent on fluorophore concentration. Also, no energy is lost during internal conversion, since internal conversion is an isoenergetic process. The excitation energy is lost during the vibrational relaxation process that takes place after the internal conversion process.
@microbio82
@microbio82 9 жыл бұрын
that was great, i like it so much, it helps so much... thank so much for all of this great demonstration and information thaaaaaaaaank u sir
@antoniosong96
@antoniosong96 4 жыл бұрын
These videos are amazing. Thank you
@mehulsharma5228
@mehulsharma5228 9 жыл бұрын
at 16:02, he says that there's an intereference of light. what causes the phase difference for interference to occur ?
@ninahaindl2221
@ninahaindl2221 2 жыл бұрын
Perfect video!!! Thanks so much
@trubit7372
@trubit7372 4 жыл бұрын
Thank you for the education on fluorescence microscopy. I need to capture a live video of bacteria reaction/dying in presence of house hold disinfectant such as Clorox and Lysol drops. What equipment is best for capturing the video? Would a LED based Dark-field Microscope be good enough or should I consider buying a Fluorescence Microscope and if so what is a good cheaper brand I should look at?
@GolamRabbiChemistry
@GolamRabbiChemistry 4 жыл бұрын
i have a question. Actually which electron will go upper state. Here the higher energy state of which molecule? If single electron go up, then sometime spin change, why?
@juanodasso5740
@juanodasso5740 26 күн бұрын
Great video. Thanks
@HM-diszt
@HM-diszt 6 жыл бұрын
Very well explained, thank you so much!
@sochummy
@sochummy 10 жыл бұрын
great explanation! thank you!
@AKLM24
@AKLM24 4 ай бұрын
Gratefully, thank you ❤❤❤
@siyuweinisi
@siyuweinisi 10 жыл бұрын
Great video, do you know how to clean the oil inside of the objective? Thanks.
@priyanshuanand3782
@priyanshuanand3782 5 жыл бұрын
Really awesome explanation Sir
@CataM1988
@CataM1988 4 жыл бұрын
Thank you! Very clear lecture.
@user-wo8hh5pz7o
@user-wo8hh5pz7o 2 жыл бұрын
Thank you for this video! Very helpful
@OmamaJM1
@OmamaJM1 9 жыл бұрын
> Thank You so much for uploading it
@TaniaSBonny
@TaniaSBonny 7 жыл бұрын
Thank you so much! you explained really well.
@daizhaoji1020
@daizhaoji1020 10 жыл бұрын
Perfect presentation, thank you very much
@WorldCollections
@WorldCollections 9 жыл бұрын
Really, really great! So helpful!
@danyack9660
@danyack9660 6 жыл бұрын
Great presentation, thank you!
@doctormohammadmasalha542
@doctormohammadmasalha542 4 жыл бұрын
Does immunofluorescence microscopy emits x-ray? Or gamma rays? How much immunofluorescence microscop safe??
@CarlosDuarte2007
@CarlosDuarte2007 4 жыл бұрын
Great video!
@littleniky25
@littleniky25 10 жыл бұрын
Love it, thanks Nico! :)
@vicentemirallesliborio3573
@vicentemirallesliborio3573 3 жыл бұрын
excellent video!! thank you!
@10031972
@10031972 9 жыл бұрын
this is really helpful. But please help me how i can adjust emission and excitemnt wavelength 490 to 550nm. And how can i adjust the contrast to make the background totally dark. Please help!! I dont know anything about fluorescent microscope and really i am in need!!!!
@djalitanaful
@djalitanaful 8 жыл бұрын
hi there, I would like to know about the protein in jelly fish that you can inject into organelles, how does that work. do you have any video you can upload please? thanks
@greza5710
@greza5710 11 жыл бұрын
can you explain a negative stoke shift?
@dulanjalirodrigo7035
@dulanjalirodrigo7035 4 жыл бұрын
what is the name of the multiple cube holder?
@laurasofiaarango4890
@laurasofiaarango4890 3 жыл бұрын
Muchas gracias, muy útil, muy amable, muy bien explicado
@RahatAli_1998
@RahatAli_1998 Жыл бұрын
Incredible ! Than you
@abc-db4nu
@abc-db4nu 6 жыл бұрын
what is differance between Fluorescence imaging and florescence microscopy
@sahajgupta5225
@sahajgupta5225 5 жыл бұрын
microscopy is a part of imaging ! bioimaging is a wide approach for diagnosis and molecular studies, which includes microscopy, x ray imaging etc etc
@harpreet157
@harpreet157 9 жыл бұрын
great video tutorial for a starter. Explains really well and elaborated. I appreciate. One thing I need to know is about the bandwidth concept. What is the narrowest bandwidth we can use? SO, is it good to use as narrow range as possible?
@akeelabbas28
@akeelabbas28 9 жыл бұрын
Harpreet Kaur hey very good question, it is not about how narrow the bandwidth is, because you need to get as much of the emitted photons as possible (that is the 2nd peak in the graph). Therefore you use a bandwidth that covers as much (wider) of the emitted as possible, without covering the exciting light that you put initially (the first peak in the graph). so to keep it short look at the graph he has in 22:00 and see how the bandwidth is covering as much of the emitted as possible and as little of the exciting as possible. hope that helps
@harpreet157
@harpreet157 9 жыл бұрын
yes. It makes sense. Thanks
@sigfridshayo4715
@sigfridshayo4715 6 жыл бұрын
Well presented, thank you
@ishakashyap6974
@ishakashyap6974 3 жыл бұрын
Excellent!
@amit88033
@amit88033 Жыл бұрын
Amazing!!!
@APC-pm2on
@APC-pm2on 10 жыл бұрын
good video! p.s did you have a haircut between the scenes? :D
@erikvartiainen9615
@erikvartiainen9615 3 жыл бұрын
You cannot really claim FM to be quantitative, because in most cases what you are imaging is the fluorescent labels you have added to your sample.
@opposinn
@opposinn 9 жыл бұрын
Thanks.. awesome video!
@jkr4807
@jkr4807 9 жыл бұрын
why dying inner cell and extracellular ?
@VictorFursov
@VictorFursov 7 жыл бұрын
Thank you for nice video.
@xingbohe7067
@xingbohe7067 7 жыл бұрын
thanks for your video
@zahraeslamisamarin9394
@zahraeslamisamarin9394 3 жыл бұрын
Thank you very much
@swethagajula9154
@swethagajula9154 3 жыл бұрын
Thank you
@abelhapedras
@abelhapedras 8 жыл бұрын
thanks for the video!
@campusentertainmentbd6156
@campusentertainmentbd6156 9 жыл бұрын
good one
@deepikaosmania
@deepikaosmania 6 жыл бұрын
bbbeautiful sir
@aneilyly3911
@aneilyly3911 Күн бұрын
VIVA LA CIENCIA!
@isworos
@isworos 10 жыл бұрын
that's my uncle :)
@miaoqinghe2211
@miaoqinghe2211 4 жыл бұрын
很棒啊
@CoLocalizationRS
@CoLocalizationRS 7 жыл бұрын
You can analyze colocalization in fluorescence microscopy images on iPad using CoLocalizer app, free from App Store: itunes.apple.com/app/colocalizer-for-ipad/id1116017542?l=en&mt
@AartiNandrekar
@AartiNandrekar 10 жыл бұрын
helpfulvideo
@niakania7199
@niakania7199 5 жыл бұрын
good
@disturbingdevelopment4308
@disturbingdevelopment4308 4 жыл бұрын
Rutger Hauer between acting jobs.
@m7mdtheo
@m7mdtheo 3 жыл бұрын
👍🏻♥️
@lotharmayring6063
@lotharmayring6063 11 ай бұрын
unsharp images for much money
@IlmiMulhid
@IlmiMulhid 2 жыл бұрын
IGNOU BSCBCH 😁😊🚩
@synterr
@synterr 5 жыл бұрын
Fluorescence die during experiment ;P
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