This video aims to describe how confocal microscope works and how it is different from fluorescence microscope
Пікірлер: 93
@SaganIII5 жыл бұрын
I love the background sound “Boah”
@animatedbiologywitharpan5 жыл бұрын
Ha ha ha....... that sounds funny
@ASITV3 жыл бұрын
this sound improves my focus on confocal microscopy
@georgesaide29537 жыл бұрын
Very informative, and well said. Thank you!
@harshoza13996 жыл бұрын
Beautifully explained. Can you upload a video explaining Phase contrast microscopy? Please....
@rydeen5034 жыл бұрын
This was great information. Thanks for taking time to explain how Confocal Microscopy works!
@animatedbiologywitharpan4 жыл бұрын
Watch this one kzbin.info/www/bejne/fHvFn5Kbjd90atE
@animatedbiologywitharpan4 жыл бұрын
Please share among friends and help me to reach big audience
@bsp1275 жыл бұрын
This was an excellent explanation of this technology. Well done. Thank you very much!
@animatedbiologywitharpan5 жыл бұрын
Please rever to my another video for better explanation kzbin.info/www/bejne/fHvFn5Kbjd90atE
@animatedbiologywitharpan5 жыл бұрын
If like my explanation please share among friends and help me to reach big audience
@JohnTaylor-nk8cp3 жыл бұрын
This is beautifully explained, thank you so much. Phenomenal video
@animatedbiologywitharpan3 жыл бұрын
Please share my channel link with your friends and help me to reach big audience
@Jindy24 жыл бұрын
Excellent! Clear and concise. Many thanks.
@animatedbiologywitharpan4 жыл бұрын
There is a second part to it .... watch my microscopy playlist
@animatedbiologywitharpan4 жыл бұрын
Please share among your friends
@saakshibhayana15326 жыл бұрын
Very useful. Could easily understand for the very first time. Thanks a lot. :)
@animatedbiologywitharpan6 жыл бұрын
thanks, more videos would be uploaded soon on confocal microscopy and image analysis
@vladimirkesaev68182 жыл бұрын
A good explanation for a quick first introduction. A minor inaccuracy on the energy level diagram. Thanks and continue, please.
@animatedbiologywitharpan2 жыл бұрын
Thanks for your feedback and suggestions. Here is an updated version of the same video kzbin.info/www/bejne/fHvFn5Kbjd90atE
@sumitborhade31786 жыл бұрын
The formula should be D= 1.22 lambda/ 2 X NA, right?
@adamsmith4677 жыл бұрын
Very well explained
@deepakkakara234 жыл бұрын
Thank you, you made it easy to understand
@animatedbiologywitharpan4 жыл бұрын
Please share my channel link in your college group
@atefalmalky92687 жыл бұрын
thank you
@naomi58175 жыл бұрын
Awesome explanation, thanks!
@animatedbiologywitharpan5 жыл бұрын
Glad to know it’s helpful.... share among friends....
@animatedbiologywitharpan5 жыл бұрын
kzbin.info/www/bejne/fHvFn5Kbjd90atE in case you want details
@maiwennlilas96623 жыл бұрын
Very good! thank you!!
@animatedbiologywitharpan3 жыл бұрын
Please share my channel link with your friends and help me to reach big audience
@WillXing3 жыл бұрын
This is a great introduction of the principle of confocal microscope. However, there is a mistake from 10:00 when you calculate the pinhole diameter using point spread function: D= 1.22λ/NA - this is the size of the illumination point on your sample, not the physical pinhole diameter. For physical diameter of the pinhole, it need to be multiplied by magnification (of the objective), which give the optimal pinhole diameter D = M x (1.22λ/NA), where M is the magnification of the objective lens you use with your confocal (x60, x100,etc). It is worth to point this out in case mislead people who are studying or developing system related to confocal microscopy. Overall, great video, pretty clear and straightforward explanation. Thanks for sharing:)
@animatedbiologywitharpan3 жыл бұрын
Thanks for giving a detailed feedback.
@konradoization2 жыл бұрын
Thanks for pointing that out! - I was already wondering how such super-small pinholes with diameters of 500 nm would be realized mechanically.. Otherwise thanks for the great video arpan! :)
@pacher725 жыл бұрын
It helped a lot thank you so much
@animatedbiologywitharpan5 жыл бұрын
There is another video in the playlist named confocal microscopy details......do watch that as well
@animatedbiologywitharpan5 жыл бұрын
Might be helpful
@hendahmad95106 жыл бұрын
Well said Thanks
@animatedbiologywitharpan6 жыл бұрын
Watch the second video about confocal for details
@karcicegi53665 жыл бұрын
Thank you so much
@animatedbiologywitharpan5 жыл бұрын
There is an advance version of this
@animatedbiologywitharpan5 жыл бұрын
Check my playlist...might be useful
@abigailparry32645 жыл бұрын
Literally a blessing
@animatedbiologywitharpan5 жыл бұрын
Watch this part 2 of that video as well kzbin.info/www/bejne/fHvFn5Kbjd90atE
@animatedbiologywitharpan5 жыл бұрын
Share among friends and help them as well
@MrNailbrain4 жыл бұрын
If an electron goes from S0 to S1 and then back shouldn't it emmit the same light as it absorbs? What happens to the 21nm worth of light/energy?
@chantalusai32423 жыл бұрын
There is an error there, there should be other vibrational states higher than S1 and the blue arrow should land there, hence the Energy difference. 😅
@rockhardX4 жыл бұрын
Set for my presentation thank you
@animatedbiologywitharpan4 жыл бұрын
Do watch another video on confocal from my microscopy playlist....it’s a detailed one...share among your friends and help me to reach big audience
@animatedbiologywitharpan4 жыл бұрын
Feel free to get in touch if you need help
@nabhasjyothis43734 жыл бұрын
This helped me a lot..thnks
@animatedbiologywitharpan4 жыл бұрын
There is a detailed video on same topic and I suggest you watch it
@animatedbiologywitharpan4 жыл бұрын
Please share among your friends and help me to reach big audience
@shailenderrajput35004 жыл бұрын
U my friend is a treasure which must be save
@animatedbiologywitharpan4 жыл бұрын
Ok I see
@animatedbiologywitharpan4 жыл бұрын
i dont completely understand the comment is sarcastic or genuine. But anyway if you find the content useful please share among your friends and help me to reach big audience
@dipayanbairagi6166 жыл бұрын
saved me from spending one hour on a book chapter.
@user-nx7hs7kz3l Жыл бұрын
agreed! >
@nithyasahayarubi36664 ай бұрын
Thank you so much sir
@animatedbiologywitharpan4 ай бұрын
Could you please help me by sharing my contents with your friends group/ college group. I put huge efforts in making these videos but unfortunately not a lot of people are watching this.
@nithyasahayarubi36663 ай бұрын
@@animatedbiologywitharpan ofcourse sir
@jessimay9874 жыл бұрын
Does anybody know the max resolution and magnification for this type of microscope?
@animatedbiologywitharpan4 жыл бұрын
Theoretically it can separate 2 points that are 200nm apart
@animatedbiologywitharpan4 жыл бұрын
Practically with higher na objective it and if you use 488 lazer to illuminate do it would be roughly 300 nm
@jessimay9874 жыл бұрын
Thank you!
@beardog65692 жыл бұрын
Dude has mad drawing skills
@animatedbiologywitharpan2 жыл бұрын
Please share my channel link with your friends and juniors
@amitkhatti68076 жыл бұрын
Well explained
@animatedbiologywitharpan6 жыл бұрын
Soon I would upload a detailed video on confocal
@animatedbiologywitharpan6 жыл бұрын
kzbin.info/www/bejne/fHvFn5Kbjd90atE
@yiyiyao71655 жыл бұрын
great explanation and very helpful! but the noises in the background are a little distracting
@animatedbiologywitharpan5 жыл бұрын
kzbin.info/www/bejne/fHvFn5Kbjd90atE
@animatedbiologywitharpan5 жыл бұрын
This video is the second part and better one
@animatedbiologywitharpan5 жыл бұрын
Don’t forget to share among friends and thanks for suggestions
@lotharmayring60632 ай бұрын
a normal achromat is confocal if you use a pinhole
@Bio-tec6 жыл бұрын
Reduce back ground disturbance.
@user-hd7pn2is3k4 жыл бұрын
if both my professor and you drown in water i shall save you first
@animatedbiologywitharpan4 жыл бұрын
Eugene Moon please share among your friends
@animatedbiologywitharpan4 жыл бұрын
Eugene Moon but you should have watched the advanced version of this video not this one ....it too much basics .Please watch the following kzbin.info/www/bejne/fHvFn5Kbjd90atE
@user-hd7pn2is3k4 жыл бұрын
@@animatedbiologywitharpan i needed to learn from the crude basics, but thank you anyways :) i will watch your recommendation too thanx!!
@sakshisood71084 жыл бұрын
Please use ur own accent..U already have a good one..Otherwise good video..Thanks
@animatedbiologywitharpan4 жыл бұрын
sakshi sood I appreciate your feedback.... it would help me to improve in future
@lg6916 жыл бұрын
"Microscopy"
@lotharmayring60632 ай бұрын
confocal must not be fluorescence
@abdalkaderali71764 жыл бұрын
Not clear
@animatedbiologywitharpan4 жыл бұрын
kzbin.info/www/bejne/fHvFn5Kbjd90atE Please watch this video...it would be clear
@hitikapuri73885 жыл бұрын
So irritating background noise.....aaahhhhhhhhhh
@animatedbiologywitharpan5 жыл бұрын
There is another video which don't have this back ground noise called " confocal microscopy details "