Team:Groningen/protocols/PCR
From 2013.igem.org
(Difference between revisions)
Line 30: | Line 30: | ||
<li>DNTPs</li> | <li>DNTPs</li> | ||
<li>Phusion buffer</li> | <li>Phusion buffer</li> | ||
- | <li> | + | <li>MQ water</li> |
<li>Phusion Polymerase</li> | <li>Phusion Polymerase</li> | ||
<li>DNA template</li> | <li>DNA template</li> |
Revision as of 10:47, 27 July 2013
PCR
Materials:
- PCR tubes
- F- and R-primer
- DNTPs
- Phusion buffer
- MQ water
- Phusion Polymerase
- DNA template
Steps:
Component | 50μl reaction | Final concentration |
H2O | up to 50μl | |
5x Phusion Buffer | 10μl | 1x |
10mM dNTPs | 1μl | 200μM |
F-primer | 1μl | 0.2μM |
R-primer | 1μl | 0.2μM |
Template DNA | 1μl | ~1ng |
Phusion Pol. 2U/μl | 0.5μl | 0.02U/μl |
Cycling instructions:
Temperature | Time | Number of cycles |
98°C | 30sec | 1 |
98°C | 10sec | 30 |
primer annealing temperature | 30sec | |
72°C | 30sec/kb | |
72°C | 10min | 1 |
4°C | ∞ | 1 |
Reference: http://www.thermoscientificbio.com/uploadedFiles/Resources/f-530s-product-information.pdf