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PCR | Polymerase Chain Reaction | Video 3

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In 1986, a technique, called the polymerase chain reaction (PCR), was developed. PCR is a rapid method of DNA cloning that extends the power of recombinant DNA and in many cases eliminates the need to use host cells for cloning. PCR is a method of choice for many applications, whether in molecular biology, human genetics, evolution, development, conservation, or forensics. PCR Reagents are pre-requisite of reaction. Reagents include Template DNA, Primers, DNTP's, Taq Polymerase, PCR Buffer and MgCl2 which is a cofactor for Taq polymerase.
PCR is performed in three steps.
1) Denaturation
2) Annealing
3) Extension or Elongation.
PCR is performed in three steps.
1) Denaturation
2) Annealing
3) Extension or Elongation.
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