Difference between revisions of "Team:Warwick/Modelling1"

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<h4>DNA Origami Glue Sequences</h4>
 
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The right shows the sequences and linkers which we will use.
 
<br><b>Procedure</b>
 
<br>1) Remove insert from plasmid
 
<br>2) PCR the plasmids
 
<br>3) Use restriction enzymes to cut the plasmids into smaller pieces of equal length (150 bp)
 
<br>4) Create "linker" DNA
 
<br>5) Denature the double stranded DNA and add linkers
 
<br>6) Allow to cool and be amazed at the results
 
 
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Revision as of 17:55, 16 September 2015