+Andrew Areva We re-recorded this video a couple of years ago with higher resolution. Check it (and a lot of other microscopy videos) here: ua-cam.com/video/1Q5V442V7xI/v-deo.html
Really nice video, thanks for uploading this. I suggest this to anyone who is going to use a confocal as its going to make your life a lot easier and will make it all a lot clearer. Thanks
awesome vid, thanks to iBiology and Nikon! Wish the resolution was higher though. Crazy to think that after a few years (from the date of this video in 2010) laser scanning confocal has gotten so efficient with the new generation of insanely fast galvano-resonance hybrid scanners that spinning disk is getting phased out since you can get pretty much very close frame rates at comparable resolutions (something like 30 fps, 512x512) without the small compromise in optical sectioning that you get in spinning disk (which is not as bad as some people make it out to be though). Although 2-photon's still the boss, if you've got the $$$$$$ hehe
Thank you for the very helpful video. I have one question.1. Why do we limit to 100µm imaging depth by confocal microscopy? Does imaging depth get better by decreasing pinhole size?
excellent video..i have a question please,i want to do a fluorescent exerience with confical and 1 EMCCD camera ..what is the difference between using 2 camera or 2 ...thank you
I am stuck, can't get it. trying hard to understand how to see molecular interactions using fluorescence and confocal microscope. is there any possibility to do a video before this and explain basics of how light interacts with specimen?
Extremely thorough and well-prepared discussion of a topic in which I had no previous understanding. Totally great!
That's just extra ordinary talent. To make such a complicated thing so simple
If only this video was in higher resolution...
+Andrew Areva We re-recorded this video a couple of years ago with higher resolution. Check it (and a lot of other microscopy videos) here: ua-cam.com/video/1Q5V442V7xI/v-deo.html
@@scicommlab Great use of super-resolution imaging 👀
try confocal
Really nice video, thanks for uploading this. I suggest this to anyone who is going to use a confocal as its going to make your life a lot easier and will make it all a lot clearer. Thanks
Thank you so much for this excellent presentation!!! ❤
Thanks for an excellent, easy to follow introduction to confocal microscopy! That would have taken me hours to read:) Keep up the great work.
Excellent video. Very easy to follow. Thank you!
awesome vid, thanks to iBiology and Nikon! Wish the resolution was higher though.
Crazy to think that after a few years (from the date of this video in 2010) laser scanning confocal has gotten so efficient with the new generation of insanely fast galvano-resonance hybrid scanners that spinning disk is getting phased out since you can get pretty much very close frame rates at comparable resolutions (something like 30 fps, 512x512) without the small compromise in optical sectioning that you get in spinning disk (which is not as bad as some people make it out to be though). Although 2-photon's still the boss, if you've got the $$$$$$ hehe
Thank you for the very helpful video. I have one question.1. Why do we limit to 100µm imaging depth by confocal microscopy? Does imaging depth get better by decreasing pinhole size?
Excellent presentation, very didactic, thanks Kurt
Thank you. Very precise and informative.
thank you
13:45 Apparatus.
18:28 Spinning disk.
22:30 Multi-photon.
excellent video..i have a question please,i want to do a fluorescent exerience with confical and 1 EMCCD camera ..what is the difference between using 2 camera or 2 ...thank you
Thanks for this wonderful video
Very helpful, thanks!
I am stuck, can't get it. trying hard to understand how to see molecular interactions using fluorescence and confocal microscope. is there any possibility to do a video before this and explain basics of how light interacts with specimen?
is there a difference between the dichromatic mirror and dichrioic mirror?
this is such a good one! Thank you so much
Thank you so much!!
Thank you is very much for the video!
Thank you for making this video.
Very nice presentation there. However, if it was in HD (720p or better), I would have seen and maybe understood more ;)
Fantastic. Very well explained.
Excellent presentation!
Good explanation of the diagrams. Thank you!
wait.. working of spiral spinning disc is not very clear..
Excellent work Kurt!!! I've addad a link on my blog -
Thank You very much
Confocal and multi-photon way to go! Spent years in research using, and later selling LOL!
Thanks, Thanks ! So great video.
Great help. Thanks!
Thanks for great explanation
very helpful, thank you :)
a life saver !
Very nice video! thanks for uploading :)
explained very clear.
Excellent!
Great video.
Thank you!
need elctron microscope for hiv diagnoses
Confocal Microscopy starts at 3:50
fantastic!!
very clear... helped me a lot... thanks..:)
Awesome!
yes... Awesome!
spinning spiral mirror working is not very clear
Great! Thanks
Nice one!
Excelente! Muchas gracias, esto me ayudó mucho. :-)
awesome!
very interesting thanks
hell yes
Thanks a lot
Opino. Que. Diyegnnoñojia. Es. Maravillosa. Pero. Soy. Una. Simple. S🎃😊😅😂😂
LIKE.
If only microscopists and histology people added scale bars. Don't show me an image without context!
like
unsharp unsharp unsharp unsharp unsharp ..................................
Why is this potato quality?
uploaded 5+ years ago. UA-cam had harsher compression requirements back then.
also, probably an old camera
"you can see that there is stuff that is clear and sharp and in focus.." yeah.. nah not really :'D
Thank you so much for this excellent presentation!!! ❤
Thank you so much!!
Very helpful, thanks!
Awesome!
Awesome!