Team:Evry/Protocols
From 2012.igem.org
(Difference between revisions)
Line 90: | Line 90: | ||
<td>72°C</td> | <td>72°C</td> | ||
<td>10min</td> | <td>10min</td> | ||
- | <td rowspan=" | + | <td rowspan="2">1</td> |
</tr> | </tr> | ||
<tr> | <tr> |
Revision as of 13:03, 3 August 2012
Contents |
PCR with Phusion High-Fidelity DNA Polymerase
Tube preparation
Put items in this order:
Component | 50µl reaction | Comments |
H2O | 32 | |
5x Phusion HF Buffer | 10 | |
10mM dNTPs | 1 | |
Primer FW | 2 | Primers have to be at 10µM |
Primer RV | 2 | Primers have to be at 10µM |
Template DNA | 1 | |
DMSO (optional) | 1,5 | recommended for GC-rich amplicons < 20kb |
Phusion DNA polymerase | 0,5 |
Cycling instructions
Cycle step | Temperature | Time | Cycles |
Initial denaturation | 98°C | 4min | 1 |
Denaturation | 98°C | 20s | 30 |
Annealing | Lower Tm of primers | 30s | |
Extension | 72°C | 30S/kb | |
Final extension | 72°C | 10min | 1 |
4°C | hold |
Préparation of LB medium and LB Agar:
=> LB Agar :
-18,5g LB Agar
-300ml H2O
=> LB medium : -6g LB broth -300ml de H2O
Autoclaved at 250°C