Linear plasmid-9

 During the extraction, putting the rest of the samples on a gel was not able to see anything. All that was on the gels was a smear. So to see if there was anything that could be done to purify, so we ran a heat gradient of the fragments of right & tet and added left. This was then run from 64-36*C. During this there was also a plasmid extraction done, this gave us a side project confirmation from this plasmid.