Team:Macquarie Australia/Protocols/Ligation
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<h1>Ligation Procedure</h1> | <h1>Ligation Procedure</h1> | ||
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+ | .datagrid {border-collapse: collapse; text-align: left; width: 100%;} .datagrid {font: normal 12px/150% Verdana, Arial, Helvetica, sans-serif; background: #fff; overflow: hidden; }.datagrid table td, .datagrid table th { padding: 3px 12px; }.datagrid table thead th {background:-webkit-gradient( linear, left top, left bottom, color-stop(0.05, #991821), color-stop(1, #80141C) );background:-moz-linear-gradient( center top, #991821 5%, #80141C 100% );filter:progid:DXImageTransform.Microsoft.gradient(startColorstr='#991821', endColorstr='#80141C');background-color:#991821; color:#FFFFFF; font-size: 14px; font-weight: bold; border-left: 1px solid #B01C26; } .datagrid table thead th:first-child { border: none; }.datagrid table tbody td { color: #000000; border-left: 1px solid #DBDBDB;font-size: 12px;font-weight: normal; }.datagrid table tbody .alt td { background: #303030; color: #FFFFFF; }.datagrid table tbody td:first-child { border-left: none; }.datagrid table tbody tr:last-child td { border-bottom: none; } | ||
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+ | <thead><tr><th>Element </th><th>Volume</th></tr></thead> | ||
+ | <tbody><tr><td>Upstream Digestion part </td><td>2 µL</td></tr> | ||
+ | <tr class="alt"><td>Downstream Digestion part</td><td>2 µL</td></tr> | ||
+ | <tbody><tr><td>Destination Plasmid</td><td>1 µL</td></tr> | ||
+ | <tr class="alt"><td>10X T4 DNA ligase buffer</td><td>2 µL</td></tr> | ||
+ | <tbody><tr><td>T4 DNA ligase</td><td>1 µL</td></tr> | ||
+ | <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 part | 2 µL |
Destination Plasmid | 1 µL |
10X T4 DNA ligase buffer | 2 µL |
T4 DNA ligase | 1 µL |
H2O | 12 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.