I have to do a work for a class about the stability of DNA in Drosophila melanogaster.
We would like to know how many time can be frozen the DNA of one sample without any kind of degration.
The same for one solution in a buffer between diferents temperatures.
To check that, we will do a PCR assuming that if we don't get amplification, the DNA has been degradated.
What temperatures would you use? Any other ideas?