Confocal microscopy Basics

  Рет қаралды 63,179

Animated biology With arpan

Animated biology With arpan

8 жыл бұрын

This video aims to describe how confocal microscope works and how it is different from fluorescence microscope

Пікірлер: 93
@SaganIII
@SaganIII 5 жыл бұрын
I love the background sound “Boah”
@animatedbiologywitharpan
@animatedbiologywitharpan 5 жыл бұрын
Ha ha ha....... that sounds funny
@ASITV
@ASITV 3 жыл бұрын
this sound improves my focus on confocal microscopy
@georgesaide2953
@georgesaide2953 7 жыл бұрын
Very informative, and well said. Thank you!
@harshoza1399
@harshoza1399 6 жыл бұрын
Beautifully explained. Can you upload a video explaining Phase contrast microscopy? Please....
@rydeen503
@rydeen503 4 жыл бұрын
This was great information. Thanks for taking time to explain how Confocal Microscopy works!
@animatedbiologywitharpan
@animatedbiologywitharpan 4 жыл бұрын
Watch this one kzbin.info/www/bejne/fHvFn5Kbjd90atE
@animatedbiologywitharpan
@animatedbiologywitharpan 4 жыл бұрын
Please share among friends and help me to reach big audience
@bsp127
@bsp127 5 жыл бұрын
This was an excellent explanation of this technology. Well done. Thank you very much!
@animatedbiologywitharpan
@animatedbiologywitharpan 5 жыл бұрын
Please rever to my another video for better explanation kzbin.info/www/bejne/fHvFn5Kbjd90atE
@animatedbiologywitharpan
@animatedbiologywitharpan 5 жыл бұрын
If like my explanation please share among friends and help me to reach big audience
@JohnTaylor-nk8cp
@JohnTaylor-nk8cp 3 жыл бұрын
This is beautifully explained, thank you so much. Phenomenal video
@animatedbiologywitharpan
@animatedbiologywitharpan 3 жыл бұрын
Please share my channel link with your friends and help me to reach big audience
@Jindy2
@Jindy2 4 жыл бұрын
Excellent! Clear and concise. Many thanks.
@animatedbiologywitharpan
@animatedbiologywitharpan 4 жыл бұрын
There is a second part to it .... watch my microscopy playlist
@animatedbiologywitharpan
@animatedbiologywitharpan 4 жыл бұрын
Please share among your friends
@saakshibhayana1532
@saakshibhayana1532 6 жыл бұрын
Very useful. Could easily understand for the very first time. Thanks a lot. :)
@animatedbiologywitharpan
@animatedbiologywitharpan 6 жыл бұрын
thanks, more videos would be uploaded soon on confocal microscopy and image analysis
@vladimirkesaev6818
@vladimirkesaev6818 2 жыл бұрын
A good explanation for a quick first introduction. A minor inaccuracy on the energy level diagram. Thanks and continue, please.
@animatedbiologywitharpan
@animatedbiologywitharpan 2 жыл бұрын
Thanks for your feedback and suggestions. Here is an updated version of the same video kzbin.info/www/bejne/fHvFn5Kbjd90atE
@sumitborhade3178
@sumitborhade3178 6 жыл бұрын
The formula should be D= 1.22 lambda/ 2 X NA, right?
@adamsmith467
@adamsmith467 7 жыл бұрын
Very well explained
@deepakkakara23
@deepakkakara23 4 жыл бұрын
Thank you, you made it easy to understand
@animatedbiologywitharpan
@animatedbiologywitharpan 4 жыл бұрын
Please share my channel link in your college group
@atefalmalky9268
@atefalmalky9268 7 жыл бұрын
thank you
@naomi5817
@naomi5817 5 жыл бұрын
Awesome explanation, thanks!
@animatedbiologywitharpan
@animatedbiologywitharpan 5 жыл бұрын
Glad to know it’s helpful.... share among friends....
@animatedbiologywitharpan
@animatedbiologywitharpan 5 жыл бұрын
kzbin.info/www/bejne/fHvFn5Kbjd90atE in case you want details
@maiwennlilas9662
@maiwennlilas9662 3 жыл бұрын
Very good! thank you!!
@animatedbiologywitharpan
@animatedbiologywitharpan 3 жыл бұрын
Please share my channel link with your friends and help me to reach big audience
@WillXing
@WillXing 3 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:)
@animatedbiologywitharpan
@animatedbiologywitharpan 3 жыл бұрын
Thanks for giving a detailed feedback.
@konradoization
@konradoization 2 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! :)
@pacher72
@pacher72 5 жыл бұрын
It helped a lot thank you so much
@animatedbiologywitharpan
@animatedbiologywitharpan 5 жыл бұрын
There is another video in the playlist named confocal microscopy details......do watch that as well
@animatedbiologywitharpan
@animatedbiologywitharpan 5 жыл бұрын
Might be helpful
@hendahmad9510
@hendahmad9510 6 жыл бұрын
Well said Thanks
@animatedbiologywitharpan
@animatedbiologywitharpan 6 жыл бұрын
Watch the second video about confocal for details
@karcicegi5366
@karcicegi5366 5 жыл бұрын
Thank you so much
@animatedbiologywitharpan
@animatedbiologywitharpan 5 жыл бұрын
There is an advance version of this
@animatedbiologywitharpan
@animatedbiologywitharpan 5 жыл бұрын
Check my playlist...might be useful
@abigailparry3264
@abigailparry3264 5 жыл бұрын
Literally a blessing
@animatedbiologywitharpan
@animatedbiologywitharpan 5 жыл бұрын
Watch this part 2 of that video as well kzbin.info/www/bejne/fHvFn5Kbjd90atE
@animatedbiologywitharpan
@animatedbiologywitharpan 5 жыл бұрын
Share among friends and help them as well
@MrNailbrain
@MrNailbrain 4 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?
@chantalusai3242
@chantalusai3242 3 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. 😅
@rockhardX
@rockhardX 4 жыл бұрын
Set for my presentation thank you
@animatedbiologywitharpan
@animatedbiologywitharpan 4 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
@animatedbiologywitharpan
@animatedbiologywitharpan 4 жыл бұрын
Feel free to get in touch if you need help
@nabhasjyothis4373
@nabhasjyothis4373 4 жыл бұрын
This helped me a lot..thnks
@animatedbiologywitharpan
@animatedbiologywitharpan 4 жыл бұрын
There is a detailed video on same topic and I suggest you watch it
@animatedbiologywitharpan
@animatedbiologywitharpan 4 жыл бұрын
Please share among your friends and help me to reach big audience
@shailenderrajput3500
@shailenderrajput3500 4 жыл бұрын
U my friend is a treasure which must be save
@animatedbiologywitharpan
@animatedbiologywitharpan 4 жыл бұрын
Ok I see
@animatedbiologywitharpan
@animatedbiologywitharpan 4 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
@dipayanbairagi616
@dipayanbairagi616 6 жыл бұрын
saved me from spending one hour on a book chapter.
@user-nx7hs7kz3l
@user-nx7hs7kz3l Жыл бұрын
agreed! >
@nithyasahayarubi3666
@nithyasahayarubi3666 4 ай бұрын
Thank you so much sir
@animatedbiologywitharpan
@animatedbiologywitharpan 4 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.
@nithyasahayarubi3666
@nithyasahayarubi3666 3 ай бұрын
@@animatedbiologywitharpan ofcourse sir
@jessimay987
@jessimay987 4 жыл бұрын
Does anybody know the max resolution and magnification for this type of microscope?
@animatedbiologywitharpan
@animatedbiologywitharpan 4 жыл бұрын
Theoretically it can separate 2 points that are 200nm apart
@animatedbiologywitharpan
@animatedbiologywitharpan 4 жыл бұрын
Practically with higher na objective it and if you use 488 lazer to illuminate do it would be roughly 300 nm
@jessimay987
@jessimay987 4 жыл бұрын
Thank you!
@beardog6569
@beardog6569 2 жыл бұрын
Dude has mad drawing skills
@animatedbiologywitharpan
@animatedbiologywitharpan 2 жыл бұрын
Please share my channel link with your friends and juniors
@amitkhatti6807
@amitkhatti6807 6 жыл бұрын
Well explained
@animatedbiologywitharpan
@animatedbiologywitharpan 6 жыл бұрын
Soon I would upload a detailed video on confocal
@animatedbiologywitharpan
@animatedbiologywitharpan 6 жыл бұрын
kzbin.info/www/bejne/fHvFn5Kbjd90atE
@yiyiyao7165
@yiyiyao7165 5 жыл бұрын
great explanation and very helpful! but the noises in the background are a little distracting
@animatedbiologywitharpan
@animatedbiologywitharpan 5 жыл бұрын
kzbin.info/www/bejne/fHvFn5Kbjd90atE
@animatedbiologywitharpan
@animatedbiologywitharpan 5 жыл бұрын
This video is the second part and better one
@animatedbiologywitharpan
@animatedbiologywitharpan 5 жыл бұрын
Don’t forget to share among friends and thanks for suggestions
@lotharmayring6063
@lotharmayring6063 2 ай бұрын
a normal achromat is confocal if you use a pinhole
@Bio-tec
@Bio-tec 6 жыл бұрын
Reduce back ground disturbance.
@user-hd7pn2is3k
@user-hd7pn2is3k 4 жыл бұрын
if both my professor and you drown in water i shall save you first
@animatedbiologywitharpan
@animatedbiologywitharpan 4 жыл бұрын
Eugene Moon please share among your friends
@animatedbiologywitharpan
@animatedbiologywitharpan 4 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-hd7pn2is3k
@user-hd7pn2is3k 4 жыл бұрын
@@animatedbiologywitharpan i needed to learn from the crude basics, but thank you anyways :) i will watch your recommendation too thanx!!
@sakshisood7108
@sakshisood7108 4 жыл бұрын
Please use ur own accent..U already have a good one..Otherwise good video..Thanks
@animatedbiologywitharpan
@animatedbiologywitharpan 4 жыл бұрын
sakshi sood I appreciate your feedback.... it would help me to improve in future
@lg691
@lg691 6 жыл бұрын
"Microscopy"
@lotharmayring6063
@lotharmayring6063 2 ай бұрын
confocal must not be fluorescence
@abdalkaderali7176
@abdalkaderali7176 4 жыл бұрын
Not clear
@animatedbiologywitharpan
@animatedbiologywitharpan 4 жыл бұрын
kzbin.info/www/bejne/fHvFn5Kbjd90atE Please watch this video...it would be clear
@hitikapuri7388
@hitikapuri7388 5 жыл бұрын
So irritating background noise.....aaahhhhhhhhhh
@animatedbiologywitharpan
@animatedbiologywitharpan 5 жыл бұрын
There is another video which don't have this back ground noise called " confocal microscopy details "
@hitikapuri7388
@hitikapuri7388 5 жыл бұрын
Thanks... tomorrow is IIT jam exam....
@animatedbiologywitharpan
@animatedbiologywitharpan 5 жыл бұрын
All the best
@hitikapuri7388
@hitikapuri7388 5 жыл бұрын
Thank u so much..
confocal vs widefield : difference in image quality
3:02
Animated biology With arpan
Рет қаралды 4,4 М.
Introduction to Confocal Microscopy
27:16
OiVM - Optical Imaging & Vital Microscopy
Рет қаралды 47 М.
How many pencils can hold me up?
00:40
A4
Рет қаралды 17 МЛН
1❤️
00:20
すしらーめん《りく》
Рет қаралды 32 МЛН
Limit of resolution and resolving power of microscope
7:29
Animated biology With arpan
Рет қаралды 78 М.
Confocal microscopy | What is the difference between confocal and fluorescence microscopy?
18:14
Confocal microscopy principle tutorial
12:18
Shomu's Biology
Рет қаралды 111 М.
The Confocal Principle
11:04
Microcourses
Рет қаралды 19 М.
Microscopy: Optical Sectioning and Confocal Microscopy (Kurt Thorn)
24:47
iBiology Techniques
Рет қаралды 48 М.
Introduction to Spinning Disk Microscopy
15:13
Teledyne Photometrics
Рет қаралды 14 М.
Fluorescence microscopy | fluorescence microscope principle
24:41
Shomu's Biology
Рет қаралды 167 М.