Team:Cambridge/Protocols/PCR
From 2011.igem.org
Contents |
Polymerase Chain Reaction (PCR)
The goal of PCR is to amplify a section of DNA of interest for DNA analysis (e.g. gene insertion, sequencing, etc). The amplification rate is exponential.
Theory
![](/wiki/images/3/3f/CAM_PCR.png)
The reaction works by the annealing of primers to single stranded DNA, which are extended by DNA polymerase. By repeating the process, the section of DNA between the primers is amplified.
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Practice
The PCR reaction contains the following reagents:
Name | Quantity |
---|---|
De-Ionized Water | 35.5 μL |
5x Buffer | 10 μL |
DNTPs | 1 μL |
Forward Primer | 1 μL |
Reverse Primer | 1 μL |
DNA Template | 1 μL |
Polymerase | 0.5 μL |
Only the primers and the DNA template are specific to the reaction. The remaining reagents can be made as a 'Master Mix' in order to reduce the need to repeatedly pipette small volumes which amplify experimental error.
As with all enzyme-containing reagents, the master mix should be kept in the freezer and small aliquots thawed when required.
The remainder of the reaction is handled automatically by a PCR machine. It is common practice to perform a gel electrophoresis to extract the correct DNA after PCR.
An example of conditions we used for a PCR reaction using Phusion polymerase are as follows:
Cycle | No. cycles | Step | Temp (C) | Time (s) |
1 | 1 | 1 | 98 | 30 |
2 | 30 | 1 | 98 | 10 |
2 | 55 | 30 | ||
3 | 72 | 2:30 | ||
3 | 1 | 1 | 72 | 5 |
4 | 50 | 1 | 4 | 99.59 (end) |
Safety
No bacteria are used during the reaction there is therefore little or no biological hazard. Nevertheless, it is important to observe correct laboratory procedure and wear appropriate clothing and gloves. PCR occurs at high temperature, and this may present a risk, depending on the PCR machine employed.