Team:Tuebingen/Notebook/Protocols/preparative-restriction
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- | <a href="https://2013.igem.org/Team:Tuebingen/Notebook/Protocols" style="font-size: | + | <a href="https://2013.igem.org/Team:Tuebingen/Notebook/Protocols" style="font-size: 18px">Back to Protocols</a> |
+ | <p> </p> | ||
+ | |||
+ | <h2>Digestion</h2> | ||
+ | |||
+ | <h3>Reagents</h3> | ||
+ | <table border="0"> | ||
+ | <colgroup> | ||
+ | <col width="80"> | ||
+ | <col width="300"> | ||
+ | </colgroup> | ||
+ | |||
+ | <tr> | ||
+ | <td style="text-align: center">10.0 µL</td> | ||
+ | <td><a href="https://www.neb.com/products/b7002-nebuffer-2">10x NEBuffer 2</a></td> | ||
+ | </tr> | ||
+ | |||
+ | <tr> | ||
+ | <td style="text-align: center">1.0 µL</td> | ||
+ | <td>100x BSA</td> | ||
+ | </tr> | ||
+ | |||
+ | <tr> | ||
+ | <td style="text-align: center">5 - 10 µg</td> | ||
+ | <td>Plasmid DNA</td> | ||
+ | </tr> | ||
+ | |||
+ | <tr> | ||
+ | <td style="text-align: center">2.0 µL</td> | ||
+ | <td>EcoRI or XbaI</td> | ||
+ | </tr> | ||
+ | |||
+ | <tr> | ||
+ | <td style="text-align: center">2.0 µL</td> | ||
+ | <td>PstI or SpeI</td> | ||
+ | </tr> | ||
+ | |||
+ | <tr> | ||
+ | <td style="text-align: center">to 100 µL</td> | ||
+ | <td>Aqua dest.</td> | ||
+ | </tr> | ||
+ | |||
+ | <tr> | ||
+ | <td style="text-align: center">1/10 vol</td> | ||
+ | <td>10X Antarctic Phosphatase</td> | ||
+ | </tr> | ||
+ | </table> | ||
+ | |||
+ | <p> </p> | ||
+ | |||
+ | <h3>Procedure</h3> | ||
+ | <p>Mix all reagents (except for Antarctic Phosphatase) in an 1.5 mL Eppendorf-tube and incubate at 37 °C over night. On the next day, heat inactivate restriction enzymes at 80°C for 20 min. Add 1/10 volume of 10X Antarctic Phosphatase and mix. Incubate at 37 °C for 15 min. Heat inactivate phosphatase at 70 °C for 5 min. Proceed with ligation (3A-Assembly).</p> | ||
</div> | </div> |
Revision as of 01:20, 4 October 2013
Preparative Restriction Digest
Back to Protocols
Digestion
Reagents
10.0 µL | 10x NEBuffer 2 |
1.0 µL | 100x BSA |
5 - 10 µg | Plasmid DNA |
2.0 µL | EcoRI or XbaI |
2.0 µL | PstI or SpeI |
to 100 µL | Aqua dest. |
1/10 vol | 10X Antarctic Phosphatase |
Procedure
Mix all reagents (except for Antarctic Phosphatase) in an 1.5 mL Eppendorf-tube and incubate at 37 °C over night. On the next day, heat inactivate restriction enzymes at 80°C for 20 min. Add 1/10 volume of 10X Antarctic Phosphatase and mix. Incubate at 37 °C for 15 min. Heat inactivate phosphatase at 70 °C for 5 min. Proceed with ligation (3A-Assembly).