Team:Groningen/protocols/PCR
From 2013.igem.org
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<li>DNA template</li> | <li>DNA template</li> | ||
</ul> | </ul> | ||
+ | |||
+ | |||
<p> | <p> | ||
<br> | <br> | ||
<h5>PCR reaction mixture:</h5> | <h5>PCR reaction mixture:</h5> | ||
- | <table | + | <table id="normal" width="60%"> |
- | <tr | + | <tr> |
- | <th >Component</th> | + | <th>Component</th> |
- | <th >50 | + | <th>50 ml</th> |
- | <th >Final concentration</th> | + | <th>Final concentration</th> |
</tr> | </tr> | ||
<tr> | <tr> | ||
- | <td | + | <td>MQ water</td> |
- | <td | + | <td>up to 50 µl</td> |
- | <td | + | <td></td> |
</tr> | </tr> | ||
<tr> | <tr> | ||
- | <td | + | <td>5x Phusion Buffer</td> |
- | <td | + | <td>10 µl</td> |
- | <td | + | <td>1x</td> |
</tr> | </tr> | ||
<tr> | <tr> | ||
- | <td | + | <td>DMSO 5%</td> |
- | <td | + | <td>1.5 µl</td> |
- | <td | + | <td></td> |
</tr> | </tr> | ||
<tr> | <tr> | ||
- | <td | + | <td>10 mM dNTPs</td> |
- | <td | + | <td>1 µl</td> |
- | <td | + | <td>200 µM</td> |
</tr> | </tr> | ||
<tr> | <tr> | ||
- | <td | + | <td>primer F</td> |
- | <td | + | <td>2.5 µl</td> |
- | <td | + | <td>0.5 µM</td> |
</tr> | </tr> | ||
<tr> | <tr> | ||
- | <td | + | <td>primer R</td> |
- | <td | + | <td>2.5 µl</td> |
- | <td | + | <td>0.5 µM</td> |
</tr> | </tr> | ||
<tr> | <tr> | ||
- | <td | + | <td>template DNA</td> |
- | <td | + | <td>1 µl</td> |
- | <td | + | <td>∼1 ng</td> |
</tr> | </tr> | ||
<tr> | <tr> | ||
- | <td | + | <td>Phusion Polymerase <br>2 U/µl</td> |
- | <td | + | <td>0.3 µl</td> |
- | <td | + | <td>0.01 U/µl</td> |
</tr> | </tr> | ||
Line 99: | Line 101: | ||
<br> | <br> | ||
<h5>Cycling instructions:</h5> | <h5>Cycling instructions:</h5> | ||
- | <table | + | <table id="normal" width="60%"> |
<tr> | <tr> | ||
- | <th | + | <th>Temperature</th> |
- | <th | + | <th>Time</th> |
- | <th | + | <th>Number of Cycles</th> |
</tr> | </tr> | ||
<tr> | <tr> | ||
- | <td | + | <td>98°C</td> |
- | <td | + | <td>2 min</td> |
- | <td | + | <td>1</td> |
</tr> | </tr> | ||
<tr> | <tr> | ||
- | <td | + | <td>98°C</td> |
- | <td | + | <td>10 sec</td> |
- | <td rowspan="3" | + | <td rowspan="3">34</td> |
</tr> | </tr> | ||
<tr> | <tr> | ||
- | <td | + | <td>T<sub>m</sub>-5°C</td> |
- | <td | + | <td>25 sec</td> |
</tr> | </tr> | ||
<tr> | <tr> | ||
- | <td | + | <td>72°C</td> |
- | <td | + | <td>30 sec/kb</td> |
</tr> | </tr> | ||
<tr> | <tr> | ||
- | <td | + | <td>72°C</td> |
- | <td | + | <td>10 min</td> |
- | <td | + | <td>1</td> |
</tr> | </tr> | ||
<tr> | <tr> | ||
- | <td | + | <td>4°C</td> |
- | <td | + | <td>∞</td> |
- | <td | + | <td>1</td> |
</tr> | </tr> | ||
</table> | </table> |
Latest revision as of 23:25, 4 October 2013
PCR
Materials:
- PCR tubes
- MQ water
- DMSO 5%
- Phusion buffer
- DNTPs
- F- and R-primer
- Phusion Polymerase
- DNA template
PCR reaction mixture:
Component | 50 ml | Final concentration |
---|---|---|
MQ water | up to 50 µl | |
5x Phusion Buffer | 10 µl | 1x |
DMSO 5% | 1.5 µl | |
10 mM dNTPs | 1 µl | 200 µM |
primer F | 2.5 µl | 0.5 µM |
primer R | 2.5 µl | 0.5 µM |
template DNA | 1 µl | ∼1 ng |
Phusion Polymerase 2 U/µl |
0.3 µl | 0.01 U/µl |
Cycling instructions:
Temperature | Time | Number of Cycles |
---|---|---|
98°C | 2 min | 1 |
98°C | 10 sec | 34 |
Tm-5°C | 25 sec | |
72°C | 30 sec/kb | |
72°C | 10 min | 1 |
4°C | ∞ | 1 |
Reference: http://www.thermoscientificbio.com/uploadedFiles/Resources/f-530s-product-information.pdf