PCR is a technique used to synthesize multiple copies of DNA on a template DNA that is similar to the parent DNA.
PCR depends on thermostable DNA polymerase (Taq Polymerase), and DNA primers.
Steps in PCR:
Denaturation: At temperature between 94°-95°C, denaturation of DNA occur. Parent DNA breaks and forms two strands due to the application of high temperature.
Annealing: At temperatures between 50°-56° C, DNA primers bind to separated stands.
Elongation: At a temperature of 72° C, Taq polymerase binds to primer and forms double-stranded DNA from a single strand.