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