Great explanation. One minor very mistake is that samples 14 and 15 are not in duplicate wells. If they were, you would only be able to run 39 samples in duplicate rather than 40.
Thank you, it was a very helpful info. If the positive control and the control spike seems to be higher than expected. What do I need to do? The standard are in specification and R2 =1. Please advice and thank you
Hello!! Your video helped improve my understanding a lot :) I was wondering if you'd be willing to share your references for this topic (specifically the ones used for this presentation)? I'd like to read more about it. Thank you so much!
Thx for the video! Question: How does the antigen or BSA bind to the well? is it simply through hydrophobic interaction with the polyester plate? or is there any covalent interaction between antigen and plate?
Crystal clear presentation! Thank you. Just one comment, in the last part, should the standards using antigens also (instead of any proteins), to quantify the 40 samples? In addtion, is it absorbance or fluorescence?
If you're using spectrophotometer it measures absorbance, which is what I believe they explained in this video. There are elisa methods where a flurophore is used, where fluorescence would be measured. Probably 2 years too late to answer your question though.
So interesting! Thank you! I am studying dopamine in humans and animals when active in Animal Assisted Therapy. What do you think about dopamine detected by ELISA kits from tear fluid before, during and after an intervention?
Very detailed and clear explanation including all the buffers and the reasons for different ELISA methods. Thank you!
What a helpful media! Thanks for your explanation.(Sang Jae Lee , DKU in Korea)
Thanks again! It is the fourth video from you that I watch and for the fourth time I really enjoyed a brilliant explanation.
This was super helpful! I needed to review ELISAs for my thesis project. THANK YOU!
Your explanation is so clear and great, I learned a lot from all your videos. Thank you so much and please keep up the great work !!!
Best explanation. Very descriptive. And explained the most common questions that I had.
Finally, we have a competitor of #shomusBiology. Great work.
This is so comprehensive. Thank you so much.
This is so good! thank you so much for simple comprehensive explanation and nice visuals !!
Many thanks for this very clear explanation.🌹
Praise be to LORD JESUS
Really good explanation, well understood..Thank you
thank you :))) Your channel helps me a lot when reading research papers
Incredibly helpful! Thank you 🙌
Wow this is anamazing lecture! Thank you!
Bundle of thanks ❣️ for this video.
Awesome explanation. Thank you
Very complete. Thank you.
Thank you very much for this great explanation
So...I m ready for my presentation on ELISA...Thank you so much😊😚
Great video and great explanation. Thank you
Great explanation. One minor very mistake is that samples 14 and 15 are not in duplicate wells. If they were, you would only be able to run 39 samples in duplicate rather than 40.
This is Super Helpful. Thank You!
Thank you very much, the explanation was very clear and helpful :)
Very useful videos. You made it so simple.thank u
Thank you for the clear explanation.
This was very helpful. Thank you so much.
Wow! That's a wonderful chanal. Hope it will develop.
Thank you so much for this... Really explanatory
Best video, great explanation!
this was very well put together
Back to your videos. I missed you so much.
really useful and the explanation is perfect
Thank you so much for this great video
thank you, it's so so understanable
Very clear information. Thank you
Thank you for describing very simply
very comprehensive and interesting presentation
Thank you! You’ve made it very easy to understand for entry level!
Thank you for that, i fully understood these methods which was really big problem for me.
영상 시청 완료했습니다 좋은 영상 소개 감사드립니다!!
Excellent presentation 👌
Wonderful video. Keep making videos and make them detailed explaining whatever you can in great depth. Can you please make a video on CLIA?
I have seen All your videos. Great work....
It is very helpful to understand the techniques easily.....
Thank you...😊
영양유전체학-좋은 영상 감사합니다.
I learned a lot about EILSA !! ( 식품영양학과 3학년 이세영 )
Thank you for the clear explanation
Please don’t stop making videos! You’re very helpful
Thank you, it was a very helpful info. If the positive control and the control spike seems to be higher than expected. What do I need to do? The standard are in specification and R2 =1. Please advice and thank you
Hello!! Your video helped improve my understanding a lot :) I was wondering if you'd be willing to share your references for this topic (specifically the ones used for this presentation)? I'd like to read more about it. Thank you so much!
Great video thanks a lot.👍
영양유전체학 영상 시청 완료하였습니다 좋은 영상 감사합니다.
Wonderful video 💯💯💯
soo helpful!! great work
영양유전체학 영상시청완료했습니다. 도움이 되었습니다!
very nice information shared keep it up stay blessed
Thx for the video! Question: How does the antigen or BSA bind to the well? is it simply through hydrophobic interaction with the polyester plate? or is there any covalent interaction between antigen and plate?
Thank you mam... great explanation
Thank you for doing this :D it helps a lot!!!
Crystal clear presentation! Thank you. Just one comment, in the last part, should the standards using antigens also (instead of any proteins), to quantify the 40 samples? In addtion, is it absorbance or fluorescence?
If you're using spectrophotometer it measures absorbance, which is what I believe they explained in this video. There are elisa methods where a flurophore is used, where fluorescence would be measured. Probably 2 years too late to answer your question though.
Hello ma'am
Have you stopped uploading videos?
These are genuinely really helpful and it would be great if you could continue uploading 😊
it's very detailed, thank you
Amazing explanation
So interesting! Thank you! I am studying dopamine in humans and animals when active in Animal Assisted Therapy. What do you think about dopamine detected by ELISA kits from tear fluid before, during and after an intervention?
It's pretty good, thank you so much
very helpful. Thank you
좋은 영상 감사합니다.
thanks 😊 it's really help alot ❤️
Great video and very clear explanations! (According to the lecture, the competitive ELISA should be rather indirect by its idea).
Very helpful ❤❤❤ thank you
좋은 영상 감사합니다!
영상시청하였습니니다!
이해하는데 도움이 되었습니다.
영상시청했습니다 잘봤습니다!
Great clip. Thx.
This is an amazing explanation! Thank you so much!!
Hello! Your videos are very helpful.Can to you provide videos on various molecular markers?Thank you.
Well explained!
Thank you for this lecture
Thank you very much.
Thank you mam.It was informative
Fantastic explanation!! Thank you very much!
영상 시청 했습니다 ! 도움이 되었습니다.
Hebat
Hebat
영상시청완료했습니다!
Thanks a lot!!! so helpful!!! :)
Very helpful
Very useful!
YOU'RE THE BEST
Hi
Great video
thank you ,so helpful
(영양유전체학) 영상 시청했습니다! 감사합니다
Please if you have spare time consider the possibility of making a video regarding CLIA ( Chemiluminescence )
Thanks alot so helpful
영상시청했습니다 감사합니다. (영양유전체)
Thank you !
Whats the different between capture Ab and detection Ab in Sandwich ELISA?
It was great
Thank you. This is an amazing video. Really helped me understand and write my essay
so damn usefull in the exam's rush.. thanks so much. i love u
Supr explanation🤩
thank you ma'am, God bless you !