Hi
If you run your PCR-product in an agarose gel and then extract your DNA from the gel, is the DNA after that in single or double stranded form. I want to measure the concentration in a gel so I want to know which settings I use.
Or is there a better way to measure the concentration?
Thanks a lot!
Dna after gel extraction, single or double stranded?
Started by Scienceboy, Jun 08 2011 03:23 AM
1 reply to this topic













