Thanks sir...this video has very effective explanation!!
@issaabujeries29124 жыл бұрын
You're Awesome! Thank you!
@chenellec3983 Жыл бұрын
Theoretically this makes a lot of sense... however, realistically you won't know exactly where your protein has been cleaved prior to running it on a diagonal PAGE. Wouldn't you have to purify and sequence the protein fragments following the diagonal PAGE to determine the approximate location of the disulfide bond?
@Beadesigner023 Жыл бұрын
Thank you soooooooooo much
@ahmedibrahim-mj2om6 жыл бұрын
Thank you
@akhilb76499 жыл бұрын
good one
@junczhang8 жыл бұрын
AWESOME
@paulturcott68168 жыл бұрын
I was under the impression that with SDS-PAGE the proteins are trapped in the gel, making it useful for reference and characterization, but not for physical separation and further purification?
@paulturcott68168 жыл бұрын
+Paul Turcott It seems like gel filtration chromatography would be a better option for this? By the way, I love these videos man. I'm using them to brush up on basics before I go back to grad school ;)