Nice presentation, we use immunoflourescence in diagnostic virology, where we use mouse monoclonal antibodies to bind to an antigen in a patient's specimen and then a goat labeled antimouse antibody binds to the antigen-antibody complex and a positive cell stains bright green due to flourescein isothiocynate staining, we also do direct immunoflorescence for quite a number of viruses.
Hello Dr. Thanks for your presentation. Could you kindly tell me the the doodle program you are using because I am a lecturer and want to use it in my presentations...Thanks in advance. Dr. Sameh
Qualitative, you aren't getting exact numbers for the fluorescence in this method but rather you are visualizing either yes there is fluorescence and so the antigen of interest is present or no fluorescence meaning its not present. In the same way western blotting gives you a yes this protein is present and allows you to see a relative amount of the presence so if the blot is bigger there is more protein, here the more fluorescence observed the greater the protein/antigen presence but it is not quantitative.
3:14 - 4:40 compares direct and indirect immunofluorescence.
It's the best video on immunofluorescence🎉
Thanks Sajid Sir
man saved my ass even after 4 years of making the video! good work fam
Sajid S, you are a great teacher, I thoroughly enjoy the clarity in your video
Nice presentation, we use immunoflourescence in diagnostic virology, where we use mouse monoclonal antibodies to bind to an antigen in a patient's specimen and then a goat labeled antimouse antibody binds to the antigen-antibody complex and a positive cell stains bright green due to flourescein isothiocynate staining, we also do direct immunoflorescence for quite a number of viruses.
Thanx brother
Thanks for the nice information as well.
This channel is a treasure ❤
More easy and more perfect for us. Thank you sir so much 🥰🥰
Concepts r delivered Crystal clear manner sir
Indian people i respect you 🤝you are everywhere know everything i m proud of you ❤
thank you :) i have an exam tomorrow and this is really helpful. :)
I have today :(
Same today🤕
Same ,my paper is tomorrow
What a perfect explanation... 👏👏👏👏Thank you
Very well explained......... thumbs up bravo
Well explained 🙌🏽
Very well explained .....Thank you sir
Thank you for such informative video, helped a lot.Looking forward for more of 'em.❤
Nice explanation 👏👏
Nicely explained
awesome...keep it up
Great explanation 👍
Good explanation 🎉🎉
I have a question, in procedure antibody binds with specific part of the cell but in direct and indirect method antibody binds with antigen, why?
thank you very much it was tooo much helpful keep teaching us
Thank you so much for this.
Simple and clear 🎉
thank you again tomorrow is my exam you explained very well
Great explanation! Thanks!! :)
thank you for the this detailed explanation
If in indirect immunofluorescence, imAb binds with primary antibodies (which we want to diagonise) ,than why we even need the antigen?
booom bastic thank you so much you save my life
Very well explained, thank you!
Most wecome
Amazing explanation
Thank you so much sir.explained very neat..
Most welcome
Fitc and tritc ke excitation and excitation wavelength kya hai?
Thanks i find it helpful😊
Really a great way. Thanks a lot.
Very well explained and the pictures were great!
Wonderfull Explanation
Thanks for your video. I have a question. Are the fluorescent antibodies synthetically produced proteins?
Yes... antibodies are produced by hybridoma technology and then coupled with fluorescent dye
Thank you @@sajidmicrobiology
Hello Dr. Thanks for your presentation. Could you kindly tell me the the doodle program you are using because I am a lecturer and want to use it in my presentations...Thanks in advance. Dr. Sameh
Weldone
Very nice sir .. good voice quality. Which mic did u use sir
Normal Samsung mobile earphones
@@sajidmicrobiology very good voice sir. And brilliant lecture.!! Very useful video.👍
Great
you saved my life thx
Very clear
Thank
tku tku tku uuuuuuu.was very helpful😍😍
Most welcome again
Can you please also explain how to quantitatively detect(antibody titer) the antibody level in serum samples using indirect IFA ?
How to calculate the Limit of Detection?
Hey just wondering what video editor/creator did you use for this video :)
Thank you so much!
Thank you. Very helpful!
Anyone else catch the 3D effect of the image at 2:55
Paper m is se Kya question askt h?
Thanks man 👍
Thanks a lot, but I have a question about this method if it is quantitatif or qualitatif or both them
Qualitative, you aren't getting exact numbers for the fluorescence in this method but rather you are visualizing either yes there is fluorescence and so the antigen of interest is present or no fluorescence meaning its not present. In the same way western blotting gives you a yes this protein is present and allows you to see a relative amount of the presence so if the blot is bigger there is more protein, here the more fluorescence observed the greater the protein/antigen presence but it is not quantitative.
Thanku sir👍
👏👏👏
Thank you so much sir.
Thank you!!
Thankyou sir 😇
👌👌👌
Most welcome shika. You can help our channel by donating small amount (Rs 5 to 100) on paytm-8830061003
Okk I will try 😇
Türkçe altyazı neden yok ya
very useful
Thanks Sajid
Super
Sir plz explain immunochromatography and hypersensitivity reactions
Sure
Easily understandable sir..need for Elisa too
Love ya
Thnkusomuch 😀
Thanks bro
thank you
Can anyone help me with the history of indirect micro immunofluorescence
Thanks
Thank u sir
thanks
👍
Hernandez Barbara Anderson Larry Jackson Gary
Thank you sir