Thank you for the explanation. However, I have 1 question regarding this method. How can we be sure that our fused activator-prey protein is folded properly or not? Improper folding might leads to false negative result by this assay.. I know it is kind of rare but in some cases fused protein fold differently.
i literally need tutorials that simple to hammer this stuff into my head, thank you very much^^
Thank you! It was very helpful.
time stamps to old video great thought and easy to understand
Good level of detail and really well explained. Thanks a lot buddy!
Thank you for the video, and especially the time stamps! Very useful and easy to understand.
Thank you! The video was really helpful :)
This is a great video! Thanks mate!
Thank you so much for this video 😊
YEET. good work buddy, thank you
Thank you very much
THANK YOU so much!!!! TT_TT
Thank you very much Sir.!!!
Thank you!
Thanks
Thank you for the explanation.
However, I have 1 question regarding this method. How can we be sure that our fused activator-prey protein is folded properly or not? Improper folding might leads to false negative result by this assay..
I know it is kind of rare but in some cases fused protein fold differently.
Actually this is one of the problems of the modern yeasth hybrid systems that I personally now dont know an answer to
yeyeet
Wow
2024 anyone?
Thank you 😊