The Polymerase Chain Reaction (PCR) is a fundamental laboratory technique used to amplify specific sections of DNA. Developed by Kary Mullis in 1983, this method allows scientists to produce millions of copies of a particular DNA sequence from a small initial sample, making it possible to study genes in detail.
PCR involves several cycles of heating and cooling, which facilitate the melting of DNA strands, annealing of primers to target sequences, and extension of new DNA strands by a DNA polymerase enzyme. Each cycle doubles the amount of DNA, leading to exponential amplification. This method is essential for analyzing microsatellites because it can isolate and expand these small, repeated sequences from a DNA sample, making them easier to study.
Applications of PCR are vast and include genetic research, medical diagnostics, forensic science, and detection of pathogens. In genetic studies, it is especially useful for amplifying microsatellites due to its precision and efficiency.
- A technique for DNA amplification
- Allows detailed study of specific genes or DNA sequences
- Key tool in genetic and forensic science