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Team:Macquarie Australia/Protocols/Ligation
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Revision as of 04:57, 29 August 2013
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.
