4 Answered Questions for the topic gel electrophoresis
07/29/19
Appropriate Buffer for electerophoresis of DNA & Protein TBE or TAE?
Which buffer is best for DNA Electrophoresis and which is best for Protein to be have a sharp bond?Considering a higher electrical conductivity compared to TAE & TBE and the generation of less...
more
07/22/19
How can I differentiate between polysaccharide bands and protein bands on SDS-PAGE?
I tried to extract bacterial polysaccharide but after running a SDS-PAGE I couldn't differentiate between the polysaccharide band and protein ones. I face a problem of moving up of the samples from...
more
05/07/19
When running a gel, what could cause a standard to run "faster" than usual?
We are running a gel on the products of a restriction digest to determine the size of an insert. We know the vector backbone size should be ~2.9kb; however, the standard appears to be running too...
more
03/14/19
Why should I degas my gel solution for polyacrylamide gels?
In protocols for polyacrylamide gel electrophoresis (PAGE) I often see instructions to degas the gel solution by putting it under vacuum for 10-15 minutes before polymerizing the gel. I usually...
more
Still looking for help? Get the right answer, fast.
Ask a question for free
Get a free answer to a quick problem.
Most questions answered within 4 hours.
OR
Find an Online Tutor Now
Choose an expert and meet online. No packages or subscriptions, pay only for the time you need.