Why is SDS-PAGE useful as an analytical tool, but not useful to purify your entire target enzyme?
Due to certain limit of cmc(critical micelle concentration) formation.
It is more useful for analytical tool for separation of protein molecule for it's gel digestion technique.
But it is less useful for it's prepative purpose for separation of larger amount of protein molecule.
Why is SDS-PAGE useful as an analytical tool, but not useful to purify your entire target...
Will our artificial enzyme,CelB-GFP, dissociate into subunits during SDS-PAGE? Why or why not?
Why do we use a ladder in SDS-PAGE gels? to determine SDS-PAGE electrical properties to determine protein size to determine nucleotide shape to determine protein shape
In the Western blot experiment, )Why are proteins treated with ionic detergent (SDS), reducing agents (DTT), and heat before SDS-PAGE Why do SDS-coated proteins migrate in an electric field? e molecular mass of myosin light chain I is approximately 22 kD, myosin heavy chain is 200 kD ane actin is 42 kD, Which proteins will migrate fastest through the gel? Why? In the Western blot experiment, )Why are proteins treated with ionic detergent (SDS), reducing agents (DTT), and heat before...
1-Define SDS-PAGE? 2-Explain why we use SDS (sodium dodecyl sulfate) in electrophoresis technique to separate proteins or nucleic acids? 3- Explain why TEMED should be the last reagent that add to the solution when preparing the gel?
You are investigating signaling pathways involved in the control of cell cycle. Why is SDS-PAGE well suited in studies of cyclin modification but not in studies of retinoblastoma pRb phosphorylation?
Why are host-based firewalls a useful tool for OS hardening?
During the total synthesis, you attempt to purify your target product by recrystallization using ethanol. You gently heat the solution until all of your crude product has dissolved. You try scratching the bottom of your flask, but that is also unsuccessful. What should you do to recover your target product so you can attempt the recrystallization again?
what would happen to the proteins in your gel if you did not add SDS-PAGE?
SDS Page: What is the purpose of running your proteins on a gel? What is the purpose of transferring them on to the nitrocellulose membrane? What direction does the protein need to travel (with regards to electrical charge) in order to bind to the membrane?
Discuss whether you think shaming is a useful tool of social control. Why or why not? Are there any negative associations with shaming? Given historically early examples of shaming, as well as a more recent example (it seems to pop up in the media from time to time), provide an example of shaming. If possible, provide a link to your recent example.include reference