Thank you sir for making ...such practical demonstration...I am a biotechnology student ....and its more helpful for me and also for various biotechnology, immunology, mol biology and biochemistry student......please make such wonderful videos for us....you are doing fantastic job thank u very much
Great demonstration!! Why do I cringe when I see your pipette tip touch the samples and then put back into the tubes though?? 😅😂 Does that mean that it’s not too sensitive?
Thank you sir for making ...such practical demonstration...I am a biotechnology student ....and its more helpful for me and also for various biotechnology, immunology, mol biology and biochemistry student......please make such wonderful videos for us....you are doing fantastic job thank u very much
Question: what is the purpose of the six "control samples" in the second well if we're using the first well as our standard/control?
Why there are not used block step and incubation during all processes are too short, usually all steps take an hour?
Where is the blocking step?
wow, you eye balling your ELISA instead of using a plate reader?
Great demonstration!!
Why do I cringe when I see your pipette tip touch the samples and then put back into the tubes though?? 😅😂
Does that mean that it’s not too sensitive?
The aliquots don't serve any DS use or may be its only for demo purposes.
It is in english. I don´t understand😥
if you don't know English ,go and learn in tagore 🤣🤣😂😂