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.
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!
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
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?
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?
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.
Very detailed and clear explanation including all the buffers and the reasons for different ELISA methods. Thank you!
This was super helpful! I needed to review ELISAs for my thesis project. THANK YOU!
Thanks again! It is the fourth video from you that I watch and for the fourth time I really enjoyed a brilliant explanation.
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.
What a helpful media! Thanks for your explanation.(Sang Jae Lee , DKU in Korea)
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
Incredibly helpful! Thank you 🙌
So...I m ready for my presentation on ELISA...Thank you so much😊😚
Wow! That's a wonderful chanal. Hope it will develop.
Wow this is anamazing lecture! Thank you!
Great video and great explanation. Thank you
Bundle of thanks ❣️ for this video.
Very complete. Thank you.
thank you :))) Your channel helps me a lot when reading research papers
This is Super Helpful. Thank You!
Very useful videos. You made it so simple.thank u
Best video, great explanation!
thank you, it's so so understanable
Awesome explanation. Thank you
really useful and the explanation is perfect
Thank you for the clear explanation.
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 very much for this great explanation
This was very helpful. Thank you so much.
Thank you very much, the explanation was very clear and helpful :)
Thank you so much for this... Really explanatory
Back to your videos. I missed you so much.
very nice information shared keep it up stay blessed
Thank you so much for this great video
this was very well put together
Excellent presentation 👌
영상 시청 완료했습니다 좋은 영상 소개 감사드립니다!!
very comprehensive and interesting presentation
Very clear information. Thank you
Wonderful video. Keep making videos and make them detailed explaining whatever you can in great depth. Can you please make a video on CLIA?
Great video thanks a lot.👍
Thank you for that, i fully understood these methods which was really big problem for me.
영양유전체학-좋은 영상 감사합니다.
Wonderful video 💯💯💯
soo helpful!! great work
Thank you for doing this :D it helps a lot!!!
Thank you for describing very simply
영양유전체학 영상 시청 완료하였습니다 좋은 영상 감사합니다.
좋은 영상 감사합니다!
좋은 영상 감사합니다.
영양유전체학 영상시청완료했습니다. 도움이 되었습니다!
Thank you for the clear explanation
Thank you mam... great explanation
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!
Thank you! You’ve made it very easy to understand for entry level!
It's pretty good, thank you so much
Great clip. Thx.
very helpful. Thank you
Thanks a lot!!! so helpful!!! :)
it's very detailed, thank you
thanks 😊 it's really help alot ❤️
이해하는데 도움이 되었습니다.
Amazing explanation
Very helpful ❤❤❤ thank you
Please don’t stop making videos! You’re very helpful
YOU'RE THE BEST
Hello ma'am
Have you stopped uploading videos?
These are genuinely really helpful and it would be great if you could continue uploading 😊
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
I have seen All your videos. Great work....
It is very helpful to understand the techniques easily.....
Thank you...😊
영상시청했습니다 잘봤습니다!
영상시청하였습니니다!
Well explained!
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 very much.
Great video and very clear explanations! (According to the lecture, the competitive ELISA should be rather indirect by its idea).
Hi
Great video
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?
Thank you mam.It was informative
Thank you for this lecture
Very useful!
thank you ,so helpful
영상시청완료했습니다!
영상 시청 했습니다 ! 도움이 되었습니다.
Hebat
Hebat
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.
Very helpful
Thank you !
Fantastic explanation!! Thank you very much!
(영양유전체학) 영상 시청했습니다! 감사합니다
Thanks alot so helpful
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.
영상시청했습니다 감사합니다. (영양유전체)
Please if you have spare time consider the possibility of making a video regarding CLIA ( Chemiluminescence )
Supr explanation🤩
Thank you!!!!!😭😭
Thanks 👍
I learned a lot about EILSA !! ( 식품영양학과 3학년 이세영 )
so damn usefull in the exam's rush.. thanks so much. i love u
thank you ma'am, God bless you !
Perfect