Polymerase chain reaction (PCR) is the technique to amplify specific sequences of DNA which is introduced by Kary Mullis in 1983.
Requirements for PCR is as below:
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Target DNA: denatured at 93 - 95°C
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PCR reaction mixture:
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Tris-HCL Buffer
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MgCl2
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KCl
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Gelatine
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4 dNTPs (deoxynucleoside triphosphates) such as: dATP, dCTP, dGTP and dTTP
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Triton-X 100
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Enzyme Taq (Thermus aquaticus) polymerase: thermostable
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Primers: should be 20-30 bps long