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!
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.
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?
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!
Finally, we have a competitor of #shomusBiology. Great work.
This is so good! thank you so much for simple comprehensive explanation and nice visuals !!
Best explanation. Very descriptive. And explained the most common questions that I had.
Thanks again! It is the fourth video from you that I watch and for the fourth time I really enjoyed a brilliant 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.
I have seen All your videos. Great work....
It is very helpful to understand the techniques easily.....
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 !!!
What a helpful media! Thanks for your explanation.(Sang Jae Lee , DKU in Korea)
Please don’t stop making videos! You’re very helpful
Back to your videos. I missed you so much.
Thank you for that, i fully understood these methods which was really big problem for me.
Great video and great explanation. Thank you
Wow! That's a wonderful chanal. Hope it will develop.
Great video and very clear explanations! (According to the lecture, the competitive ELISA should be rather indirect by its idea).
really useful and the explanation is perfect
Praise be to LORD JESUS
Really good explanation, well understood..Thank you
Incredibly helpful! Thank you 🙌
Very useful videos. You made it so simple.thank u
very nice information shared keep it up stay blessed
Thank you for the clear explanation.
So...I m ready for my presentation on ELISA...Thank you so much😊😚
Many thanks for this very clear explanation.🌹
This is so comprehensive. Thank you so much.
very comprehensive and interesting presentation
This is Super Helpful. Thank You!
Best video, great explanation!
thank you :))) Your channel helps me a lot when reading research papers
thank you, it's so so understanable
Wonderful video. Keep making videos and make them detailed explaining whatever you can in great depth. Can you please make a video on CLIA?
Thank you for doing this :D it helps a lot!!!
Thank you mam... great explanation
this was very well put together
Very complete. Thank you.
Thank you for the clear explanation
Amazing explanation
Very helpful ❤❤❤ thank you
Wow this is anamazing lecture! Thank you!
This was very helpful. Thank you so much.
Wonderful video 💯💯💯
Thank you so much for this... Really explanatory
I learned a lot about EILSA !! ( 식품영양학과 3학년 이세영 )
Hello ma'am
Have you stopped uploading videos?
These are genuinely really helpful and it would be great if you could continue uploading 😊
Excellent presentation 👌
Very clear information. Thank you
Great video thanks a lot.👍
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 helpful. Thank you
Thank you for describing very simply
YOU'RE THE BEST
Thank you very much.
soo helpful!! great work
영양유전체학-좋은 영상 감사합니다.
Thank you very much for this great explanation
Very helpful
so clear... thank you very much
이해하는데 도움이 되었습니다.
Awesome explanation. Thank you
Supr 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?
Very helpful. Thank you
Thank you so much for this great video
Thank you! You’ve made it very easy to understand for entry level!
thanks 😊 it's really help alot ❤️
it's very detailed, thank you
영양유전체학 영상 시청 완료하였습니다 좋은 영상 감사합니다.
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.
Thank you mam.It was informative
Thank you for this lecture
You can both use flat wells as concave wells actually
Great clip. Thx.
Well explained!
영상 시청 했습니다 ! 도움이 되었습니다.
Hebat
Hebat
영양유전체학 영상시청완료했습니다. 도움이 되었습니다!
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
Very useful!
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?
where i can found the next video about the Ria !!!!!!!!! i can't found it
Thanks 👍
영상시청하였습니니다!
It was great
This is an amazing explanation! Thank you so much!!
좋은 영상 감사합니다.
Hello! Your videos are very helpful.Can to you provide videos on various molecular markers?Thank you.
Thank you !
Hi
Great video
It's pretty good, thank you so much
so damn usefull in the exam's rush.. thanks so much. i love u
thank you ,so helpful
Please if you have spare time consider the possibility of making a video regarding CLIA ( Chemiluminescence )
좋은 영상 감사합니다!
Thank you. This is an amazing video. Really helped me understand and write my essay
Is these all test 4 the generation tests???
Please make videos on expression systems..
Whats the different between capture Ab and detection Ab in Sandwich ELISA?
영상시청했습니다 잘봤습니다!
Perfect
Thank you very much my lover