Microscopy: Introduction to Fluorescence Microscopy (Nico Stuurman)

Ғылым және технология

Learn more: www.ibiology.org/talks/introd...
Fluorescence is a process in which matter absorbs light and re-emits at a different wavelength. Fluorescence is widely used in biological microscopy. This lecture describes the principles of fluorescence and fluorescence microscopy.

Пікірлер: 89

  • @carposporophyte
    @carposporophyte4 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
    @sschw0069 жыл бұрын

    could not of asked for a better, well presented explanation of fluorescence. Very nicely done.

  • @elleoops777
    @elleoops7778 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

  • @poetryodia6704
    @poetryodia67042 жыл бұрын

    Thank you so much..no one has explained as good as you. Thank you iBiology🙏

  • @evanescent1000
    @evanescent10005 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.

  • @mervatel-deftar8412
    @mervatel-deftar84124 жыл бұрын

    Amazing lecture very simplified but of high level. thank you very much it was very helpful.

  • @naturephile554
    @naturephile5542 жыл бұрын

    Your way of explanation by using tools is really aid in learning....thank you for making such nice and helpful video !!!!

  • @exodusofficer
    @exodusofficer9 ай 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

    7 ай 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 ,

  • @annmaryjoseph6147
    @annmaryjoseph6147 Жыл бұрын

    Such a wonderful, in detail presentation. Thank you Sir

  • @tessahemrika7150
    @tessahemrika71509 жыл бұрын

    Thank you so much for this presentation, for the very first time I actually get it!

  • @drichhapurak
    @drichhapurak6 жыл бұрын

    very well explained,video makes clear the principle and working of Fluorescence microscopy,thanks

  • @DaruoshAghajaney
    @DaruoshAghajaney4 жыл бұрын

    Excellent lecture and demonstration. Really impressive.

  • @stephensonal4082
    @stephensonal40822 жыл бұрын

    Great, clear, and informative presentation. Thank you

  • @ReggaePhysics
    @ReggaePhysics6 ай бұрын

    It's a very complicated subject, and you are doing a good job here. Thanks

  • @HM-diszt
    @HM-diszt5 жыл бұрын

    Very well explained, thank you so much!

  • @nellyflorestapia
    @nellyflorestapia10 жыл бұрын

    Great job, well explained, thak you for everything

  • @Hitsong-Cutegirl
    @Hitsong-Cutegirl9 ай бұрын

    Thank you for knowledge. 😊❤

  • @goodluckdominique7255
    @goodluckdominique72554 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.

  • @etiennecartier1
    @etiennecartier110 жыл бұрын

    love it! At last I understand how those "cubes" really work!

  • @sebastian5671
    @sebastian5671 Жыл бұрын

    I have my first course in nanoengineering, this really helped, thanks a lot!

  • @daizhaoji1020
    @daizhaoji10209 жыл бұрын

    Perfect presentation, thank you very much

  • @sochummy
    @sochummy9 жыл бұрын

    great explanation! thank you!

  • @Gealamusic
    @Gealamusic Жыл бұрын

    thank you so much - really helped me get into my term paper about fluorescence microscopy

  • @TaniaSBonny
    @TaniaSBonny6 жыл бұрын

    Thank you so much! you explained really well.

  • @user-gq9yg3mu1r
    @user-gq9yg3mu1r2 жыл бұрын

    im korean, and i'd appreciate this video that is so intutive and well explained

  • @seaweedseaside5905
    @seaweedseaside59055 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.

  • @antoniosong96
    @antoniosong963 жыл бұрын

    These videos are amazing. Thank you

  • @danyack9660
    @danyack96605 жыл бұрын

    Great presentation, thank you!

  • @CataM1988
    @CataM19884 жыл бұрын

    Thank you! Very clear lecture.

  • @rann82
    @rann828 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

  • @haoguo2056
    @haoguo205610 жыл бұрын

    Good job. This is a very thorough lecture.

  • @WorldCollections
    @WorldCollections8 жыл бұрын

    Really, really great! So helpful!

  • @rnd9331
    @rnd93316 жыл бұрын

    haha play 32:19, he says fkd up instead of fluorescent :P Great lecture btw

  • @funyi3

    @funyi3

    5 жыл бұрын

    there should be some beeep sound

  • @neoretrodude

    @neoretrodude

    3 жыл бұрын

    I went straight to it

  • @khadijaw1630

    @khadijaw1630

    2 жыл бұрын

    i am so impressed how did you even notice that:) great attention, love that for you

  • @littleniky25
    @littleniky259 жыл бұрын

    Love it, thanks Nico! :)

  • @priyanshuanand3782
    @priyanshuanand37825 жыл бұрын

    Really awesome explanation Sir

  • @trubit7372
    @trubit73724 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?

  • @siyuweinisi
    @siyuweinisi9 жыл бұрын

    Great video, do you know how to clean the oil inside of the objective? Thanks.

  • @ninahaindl2221
    @ninahaindl22212 жыл бұрын

    Perfect video!!! Thanks so much

  • @OmamaJM1
    @OmamaJM18 жыл бұрын

    > Thank You so much for uploading it

  • @APC-pm2on
    @APC-pm2on10 жыл бұрын

    good video! p.s did you have a haircut between the scenes? :D

  • @sigfridshayo4715
    @sigfridshayo47155 жыл бұрын

    Well presented, thank you

  • @user-wo8hh5pz7o
    @user-wo8hh5pz7o Жыл бұрын

    Thank you for this video! Very helpful

  • @vicentemirallesliborio3573
    @vicentemirallesliborio35733 жыл бұрын

    excellent video!! thank you!

  • @ulisesmontero950
    @ulisesmontero9503 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.

  • @abelhapedras
    @abelhapedras8 жыл бұрын

    thanks for the video!

  • @xingbohe7067
    @xingbohe70676 жыл бұрын

    thanks for your video

  • @laurasofiaarango4890
    @laurasofiaarango48902 жыл бұрын

    Muchas gracias, muy útil, muy amable, muy bien explicado

  • @mr702s
    @mr702s4 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?

  • @opposinn
    @opposinn8 жыл бұрын

    Thanks.. awesome video!

  • @CarlosDuarte2007
    @CarlosDuarte20074 жыл бұрын

    Great video!

  • @RahatAli_1998
    @RahatAli_19984 ай бұрын

    Incredible ! Than you

  • @DMOND-qg2cg
    @DMOND-qg2cg2 жыл бұрын

    frodo teaching me biology, gotta love it

  • @djalitanaful
    @djalitanaful7 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

  • @10031972
    @100319728 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!!!!

  • @harpreet157
    @harpreet1579 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

  • @VictorFursov
    @VictorFursov6 жыл бұрын

    Thank you for nice video.

  • @ishakashyap6974
    @ishakashyap69742 жыл бұрын

    Excellent!

  • @amit88033
    @amit88033 Жыл бұрын

    Amazing!!!

  • @zhang_han
    @zhang_han3 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?

  • @mehulsharma5228
    @mehulsharma52288 жыл бұрын

    at 16:02, he says that there's an intereference of light. what causes the phase difference for interference to occur ?

  • @zahraeslamisamarin9394
    @zahraeslamisamarin93942 жыл бұрын

    Thank you very much

  • @swethagajula9154
    @swethagajula91542 жыл бұрын

    Thank you

  • @greza5710
    @greza571010 жыл бұрын

    can you explain a negative stoke shift?

  • @GolamRabbiChemistry
    @GolamRabbiChemistry3 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?

  • @campusentertainmentbd6156
    @campusentertainmentbd61568 жыл бұрын

    good one

  • @deepikakumar1430
    @deepikakumar14305 жыл бұрын

    bbbeautiful sir

  • @dulanjalirodrigo7035
    @dulanjalirodrigo70353 жыл бұрын

    what is the name of the multiple cube holder?

  • @doctormohammadmasalha542
    @doctormohammadmasalha5424 жыл бұрын

    Does immunofluorescence microscopy emits x-ray? Or gamma rays? How much immunofluorescence microscop safe??

  • @miaoqinghe2211
    @miaoqinghe22113 жыл бұрын

    很棒啊

  • @AartiNandrekar
    @AartiNandrekar9 жыл бұрын

    helpfulvideo

  • @jkr4807
    @jkr48078 жыл бұрын

    why dying inner cell and extracellular ?

  • @erikvartiainen9615
    @erikvartiainen96152 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.

  • @abc-db4nu
    @abc-db4nu5 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

  • @isworos
    @isworos9 жыл бұрын

    that's my uncle :)

  • @niakania7199
    @niakania71994 жыл бұрын

    good

  • @m7mdtheo
    @m7mdtheo2 жыл бұрын

    👍🏻♥️

  • @disturbingdevelopment4308
    @disturbingdevelopment43083 жыл бұрын

    Rutger Hauer between acting jobs.

  • @CoLocalizationRS
    @CoLocalizationRS6 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

  • @IlmiMulhid
    @IlmiMulhid Жыл бұрын

    IGNOU BSCBCH 😁😊🚩

  • @synterr
    @synterr4 жыл бұрын

    Fluorescence die during experiment ;P

  • @lotharmayring6063
    @lotharmayring60632 ай бұрын

    unsharp images for much money

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