Bunsen required for all steps.
1.Label tube with the name of the plasmid being added.
2.Locate DNA on kit plate (see iGEM distribution catalog).
3.Pierce the foil with a pipette containing 10 μl of sterilized water.
4.Mix well by taking up and releasing mixture multiple times.
5.Place the suspended DNA solution in a 1.5 ml Eppendorf, leaving on ice.
Team:Warwick/Protocols
