Team:Tuebingen/Notebook/Protocols/colony-pcr
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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> | ||
+ | |||
+ | <h3>Reagents</h3> | ||
+ | <table border="0"> | ||
+ | <colgroup> | ||
+ | <col width="80"> | ||
+ | <col width="300"> | ||
+ | </colgroup> | ||
+ | |||
+ | <tr> | ||
+ | <td style="text-align: center">0.5 µL</td> | ||
+ | <td>MgCl2 (c = 25 mM)</td> | ||
+ | </tr> | ||
+ | |||
+ | <tr> | ||
+ | <td style="text-align: center">1.0 µL</td> | ||
+ | <td>10x Taq Polymerase Buffer</td> | ||
+ | </tr> | ||
+ | |||
+ | <tr> | ||
+ | <td style="text-align: center">0.1 µL</td> | ||
+ | <td>dNTPs (2.5 mM each)</td> | ||
+ | </tr> | ||
+ | |||
+ | <tr> | ||
+ | <td style="text-align: center">0.1 µL</td> | ||
+ | <td>Oligo forward</td> | ||
+ | </tr> | ||
+ | |||
+ | <tr> | ||
+ | <td style="text-align: center">0.1 µL</td> | ||
+ | <td>Oligo reverse</td> | ||
+ | </tr> | ||
+ | |||
+ | <tr> | ||
+ | <td style="text-align: center">7.7 µL</td> | ||
+ | <td>Aqua dest.</td> | ||
+ | </tr> | ||
+ | |||
+ | <tr> | ||
+ | <td style="text-align: center">0.1 µL</td> | ||
+ | <td>Taq Polymerase (5 U/µL)</td> | ||
+ | </tr> | ||
+ | </table> | ||
+ | |||
+ | <p> </p> | ||
+ | |||
+ | <h3>Procedure</h3> | ||
+ | <ol> | ||
+ | <li>Put some PCR-tubes on ice.</li> | ||
+ | <li>The given volumes are for one single reaction of 15 µL. When checking more than one colony, repare a master mix for all colonies. Keep that master mix on ice all the time!</li> | ||
+ | <li>Transfer 10 µL of master mix in every ice-cold PCR-tube (1 PCR-tube per colony).</li> | ||
+ | <li>Usa a pipet tip for picking a colony from a fresh plate</li> | ||
+ | <li></li> | ||
+ | </ol> | ||
</div> | </div> | ||
+ | |||
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Revision as of 02:42, 4 October 2013
Colony-PCR
Back to Protocols
Reagents
0.5 µL | MgCl2 (c = 25 mM) |
1.0 µL | 10x Taq Polymerase Buffer |
0.1 µL | dNTPs (2.5 mM each) |
0.1 µL | Oligo forward |
0.1 µL | Oligo reverse |
7.7 µL | Aqua dest. |
0.1 µL | Taq Polymerase (5 U/µL) |
Procedure
- Put some PCR-tubes on ice.
- The given volumes are for one single reaction of 15 µL. When checking more than one colony, repare a master mix for all colonies. Keep that master mix on ice all the time!
- Transfer 10 µL of master mix in every ice-cold PCR-tube (1 PCR-tube per colony).
- Usa a pipet tip for picking a colony from a fresh plate