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By: Cody Alveraz Ted Dobbert Morgan Pettit
PCR By: Cody Alveraz Ted Dobbert Morgan Pettit
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What is PCR? PCR is a polymerase chain reaction that copies pieces of DNA across multiple orders of magnitude, creating thousands to millions of copies of DNA sequences. It was developed in 1983 by Kary Mullis.
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Procedures of PCR Denaturation: At F degrees the double stranded DNA melts and opens into 2 pieces of single-stranded DNA. Annealing: At medium temperatures, at around 54 degrees Celsius, the primers pair up with the single-stranded “template”. On the small length of double-stranded DNA, the polymerase attaches and starts copying the template.
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Procedures of PCR (cont.)
Extension: AT 72 degrees Celsius, where the polymerase works best, and DNA building blocks complementary to the template are coupled to the primer, making a double-stranded DNA molecule. With one cycle a segment of double-stranded DNA template is amplified into two separate pieces of double stranded DNA.
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What is good about PCR? PCR is good technique because its not expensive, rapid and a good way to get millions of copies of DNA.
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PCR Process Diagram
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PCR Machine
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