I love you for making this video. you're a true angel, please keep making these useful videos! thank you, thank you, thank youuuuu!!!!
@thebumblingbiochemist Жыл бұрын
Glad you found it helpful!
@chen-hsuanchiu32652 жыл бұрын
Very informative and I like the energy you share in the video!
@thebumblingbiochemist2 жыл бұрын
Thank you!
@muhammadkaleem4251 Жыл бұрын
Bravo. Super helpful. Thank you so much for making this video :) Thumbs UP :)
@thebumblingbiochemist Жыл бұрын
Glad to hear it - thanks!
@muhammadkaleem4251 Жыл бұрын
I have a question: What if we destain too much and the bands are too faint to be visualized, can we restain the gel with Coomassie and then destain again?
@thebumblingbiochemist Жыл бұрын
Yes
@MES-S Жыл бұрын
Thank you for sharing a wonderful information
@Darcy25312 жыл бұрын
This was super helpful!! Can you tell why we take the ratio of absorbance 590/450 while performing Bradford assay?
@thebumblingbiochemist2 жыл бұрын
Thanks! You take the ratio because it allows you to kinda normalize for background and make the standard curve linear: www.ncbi.nlm.nih.gov/pmc/articles/PMC3164080/
@jandecoole56872 жыл бұрын
very clear and correct explaination. thanks alot
@thebumblingbiochemist2 жыл бұрын
Thanks! Glad to hear it
@stefanodecler149 Жыл бұрын
Great explanation and so complete, thanks :) I have a question: How much time do you suggest to stain with R-250?
@thebumblingbiochemist Жыл бұрын
Thanks! Probably like 20 min or so - longer if you need more sensitivity but then the destain takes longer too! Microwaving can help
@MarianaAguilarMorales Жыл бұрын
can you share the volume of staining solution used and the time used at the microwave? thanks!
@thebumblingbiochemist Жыл бұрын
Just enough to cover the gel and 30s-1 min spurts usually