It is a technique that can monitor the progress of PCR reaction in real-time and simultaneously a small amount of product formed from that reaction can be quantified.
It is a highly useful process used in biotechnology and bioinformatics.
It is based on the principle of detection of increased fluorescence produced by reporter molecules.
A specific piece of DNA is amplified using PCR for producing its millions of copies so as to study it in greater detail.
Steps of PCR:
Denaturation: The DNA strand is heated to 95°C to separate the two strands.
Annealing: Binding of DNA primers at 55°C to the open ends that will act as a template for new strand formation.
Extension: Synthesis of the new DNA strand at 72°C using thermostable Taq polymerase enzyme.