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Team:Tuebingen/Notebook/Protocols/ligation
From 2013.igem.org
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| Line 34: | Line 34: | ||
<tr> | <tr> | ||
<td style="text-align: center">1 µL</td> | <td style="text-align: center">1 µL</td> | ||
| - | <td>10x Ligase | + | <td>10x T4 DNA Ligase Buffer</td> |
</tr> | </tr> | ||
<tr> | <tr> | ||
<td style="text-align: center">1 µL</td> | <td style="text-align: center">1 µL</td> | ||
| - | <td>T4 Ligase</td> | + | <td>T4 DNA Ligase</td> |
</tr> | </tr> | ||
Revision as of 01:51, 4 October 2013
Ligation
Back to Protocols
Reagents
| 20 - 50 ng | Linearized vector |
| 1 µL | 10x T4 DNA Ligase Buffer |
| 1 µL | T4 DNA Ligase |
| 5 µl (up to 5:1 molar ratio insert to vector) |
Insert DNA |
| fill up to 10 µL | Aqua dest. |
Procedure
Mix all reagents and fill up with Aqua dest. to 10 µL. Vortex and incubate at 4 °C over night. On the next day, inactivate enzymes at 70 °C for 5 min. Store at -20 °C.
