DNA amplification is the process of producing multiple copies of a specific DNA segment. This is done using the Polymerase Chain Reaction (PCR) technique. PCR is a powerful method because it can take a tiny amount of DNA and increase the number of molecules exponentially.
For example, starting with just one DNA double helix, PCR can generate billions of copies.
The key steps of PCR include:
- Denaturation: Heating the DNA to separate its two strands.
- Annealing: Cooling the DNA so primers can bind to the single strands.
- Extension: Heating the DNA so the enzyme Taq polymerase can add new nucleotides to form a complete copy.
These cycles are repeated multiple times to achieve significant DNA amplification. This is useful in various applications such as cloning, medical diagnostics, and forensic science.