Team:Groningen/protocols/PCR
From 2013.igem.org
(Difference between revisions)
Line 51: | Line 51: | ||
<tr><td>10mM dNTPs</td> | <tr><td>10mM dNTPs</td> | ||
<td>1</td> | <td>1</td> | ||
- | <td> | + | <td>200μM</td> |
</tr> | </tr> | ||
<tr><td>F-primer</td> | <tr><td>F-primer</td> |
Revision as of 09:08, 26 July 2013
PCR
Materials:
- PCR tubes
- F- and R-primer
- DNTPs
- Phusion buffer
- H2O
- Phusion Polymerase
- DNA template
Steps:
Component | 50μl reaction | Final concentration |
H2O | up to 50μl | |
5x Phusion Buffer | 10 | 1x |
10mM dNTPs | 1 | 200μM |
F-primer | 0.2μM | |
R-primer | 0.2μM | |
Template DNA | 1μl | ~1ng |
Phusion Pol. | 0.5μl | 0.02U/μl |
Cycling instructions:
Reference: http://www.thermoscientificbio.com/uploadedFiles/Resources/f-530s-product-information.pdf