Polymerase Chain Reaction

Principle

Polymerase Chain Reaction (PCR) is a molecular biology method used to amplify a small amount of genetic material (DNA or RNA), using specific primers of a target sequence.
PCR is divided into 5 steps:
- First denaturation:
- Denaturation step
- Annealing step
- Elongation step
- Final step
The 2nd, 3th and 4th steps are repeated 20-40 cycles.

Denaturation step occure between 94 and 98°C.The heat breaks the hydrogen bonds and then causes the separation of the double strand of DNA into two single strands.
Annealing step occure between 50 and 65 °C. Primers anneals to DNA simple strand by complementarity of the nitrogenized bases.
Elongation step occure between 70 and 80°C, depending on the DNA polymerase used. The polymerase synthesizes a new DNA strand complementary to the DNA template

Preparation

Mixture preparation

We use two differents polymerase for our PCR: Taq Polymerase and Q5.
As Q5 is a hight fidelity polymerase, we use it to obtain sequences without mutation (for a total of 50 μL of mixture); otherwise we use Taq Polymerase instead (for a total of 25 μL of mixture).
Afterwards, we will describe the protocol for a PCR with Q5 (total amount: 50 μL).
Note that proportion are the same with Taq Polymerase, for 25 μL or 50 μL: 1:10 of each primer, 1:5 of Buffer, 1:50 of dNTPs, 1:50 of genomic DNA and 1:100 of polymerase
Make tubes with 5 μL (1:10) of Forward primer and 5 μL (1:10) of Reverse primer for each desidered sequence.
For more details about our primers, see the corresponding page. For positive and negative controle, use primers that worked previously in the same condition of PCR.
We use primers (Primers 009 and 010) for pEntC for ou controles.
For n tubes, prepare a master mix with the following solutions:

• (n+1) x 10 μL of Q5 Buffer
• (n+1) x 1 μL of dNTPs
• (n+1) x 27,5 μL of distilled water.
• (n+1) x 0,5 μL of Q5

Note that you must take the enzyme out of -20°C just before utilisation. Split 39 μL of the master mix in each tube. Add 1 μL of genomic DNA in each tube, except in your negative controle tube. In this one, put 1 μL of distilled water instead.

Put your tubes into Thermo Cycler.

Optimisation

Number of primer

Temperature

Gel electrophoresis analysis

Principle

Electrophoresis is a method using electrical field to separate DNA or RNA sequence by size. Smaller the fragment is, the more it migrates on the gel.
Using a DNA ladder, we can know the size of DNA sequence and then check if we have the sequence we wanted.

Preparation

Analysis

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