Team:Macquarie Australia/Protocols/Ligation

From 2013.igem.org

Revision as of 04:57, 29 August 2013 by Trouch (Talk | contribs)
(diff) ← Older revision | Latest revision (diff) | Newer revision → (diff)


Ligation Procedure



A reaction mixture was prepared containing, Element Volume Upstream Digestion part 2 µL Downstream Digestion part 2 µL Destination Plasmid 1 µL 10X T4 DNA ligase buffer 2 µL T4 DNA ligase 1 µL H2O 12 µL

We incubated each ligation mix at 30°C for 30 minutes, followed by heat inactivation at 80°C for 20 minutes.

4 µL of the ligation product was transformed into 100 µL of competent E. coli, the transformants were then incubated for one hour.