Team:Warwick/Modelling1
DNA Origami Glue Sequences
BBa_K314110
Procedure
1) Remove insert from plasmid
2) PCR the plasmids
3) Use restriction enzymes to cut the plasmids into smaller pieces of equal length (150 bp)
4) Create "linker" DNA
5) Denature the double stranded DNA and add linkers
6) Allow to cool and be amazed at the results
