Team:Macquarie Australia/Protocols/Ligation

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<h1>Ligation Procedure</h1>
<h1>Ligation Procedure</h1>
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<thead><tr><th>Element </th><th>Volume</th></tr></thead>
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<tbody><tr><td>Upstream Digestion part </td><td>2 µL</td></tr>
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<tr class="alt"><td>Downstream Digestion part</td><td>2 µL</td></tr>
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<tbody><tr><td>Destination Plasmid</td><td>1 µL</td></tr>
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<tr class="alt"><td>10X T4 DNA ligase buffer</td><td>2 µL</td></tr>
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<tbody><tr><td>T4 DNA ligase</td><td>1 µL</td></tr>
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<tr class="alt"><td>H2O</td><td>12 µL</td></tr>
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A reaction mixture was prepared containing,
A reaction mixture was prepared containing,

Revision as of 05:16, 29 August 2013


Ligation Procedure

Element Volume
Upstream Digestion part 2 µL
Downstream Digestion part2 µL
Destination Plasmid1 µL
10X T4 DNA ligase buffer2 µL
T4 DNA ligase1 µL
H2O12 µL


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.