Polymerase Chain Reaction (PCR): Difference between revisions
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Polymerase Chain Reaction<ref>Hartl D. L., Ruvolo M. (2012), Genetics: Analysis of genes and genomes, Eight Edition, Jones and Bartlett learning (Chapter 2 DNA Structure and Genetic Variation)</ref> (PCR) is a technique used for the [[Amplification|amplification]] and identification of [[DNA|DNA]] or [[RNA|RNA]] of known sequence. Also see [[MRNA|mRNA]] (including [[Transcriptase|transcriptase]]). It allows scientists to produce many millions of copies of a certain DNA sequence in a couple of hours. This technique was developed by an american biochemist Kary Mullis in 1984<ref>Berg, J.M., Tymoczko, J.L. and Stryer, L. (2012). Biochemistry, 7 th Edition, New York , W.H.Freeman &amp; Co Ltd. pg 151</ref>.<br> | Polymerase Chain Reaction<ref>Hartl D. L., Ruvolo M. (2012), Genetics: Analysis of genes and genomes, Eight Edition, Jones and Bartlett learning (Chapter 2 DNA Structure and Genetic Variation)</ref> (PCR) is a technique used for the [[Amplification|amplification]] and identification of [[DNA|DNA]] or [[RNA|RNA]] of known sequence. Also see [[MRNA|mRNA]] (including [[Transcriptase|transcriptase]]). It allows scientists to produce many millions of copies of a certain DNA sequence in a couple of hours. This technique was developed by an american biochemist [[Kary Mullis|Kary Mullis]] in 1984<ref>Berg, J.M., Tymoczko, J.L. and Stryer, L. (2012). Biochemistry, 7 th Edition, New York , W.H.Freeman &amp;amp; Co Ltd. pg 151</ref>.<br> | ||
[[PCR|PCR ]]has three main stages: | [[PCR|PCR ]]has three main stages: | ||
#'''Strand Seperation''' : Heat ds[[DNA|DNA]] to 95°C for 15sto melt and seperate the strands. | #'''Strand Seperation''' : Heat ds[[DNA|DNA]] to 95°C for 15sto melt and seperate the strands. | ||
#'''Hybridisation of Primer''' : Cool to 50 - 65°C to allow [[Primers|primers]] to anneal to the DNA strands. | #'''Hybridisation of Primer''' : Cool to 50 - 65°C to allow [[Primers|primers]] to anneal to the DNA strands. | ||
#'''DNA Synthesis''' : Heat to 72°C to allow [[Elongation|elongation]] | #'''DNA Synthesis''' : Heat to 72°C to allow [[Elongation|elongation]] | ||
Revision as of 16:21, 20 October 2012
Polymerase Chain Reaction[1] (PCR) is a technique used for the amplification and identification of DNA or RNA of known sequence. Also see mRNA (including transcriptase). It allows scientists to produce many millions of copies of a certain DNA sequence in a couple of hours. This technique was developed by an american biochemist Kary Mullis in 1984[2].
PCR has three main stages:
- Strand Seperation : Heat dsDNA to 95°C for 15sto melt and seperate the strands.
- Hybridisation of Primer : Cool to 50 - 65°C to allow primers to anneal to the DNA strands.
- DNA Synthesis : Heat to 72°C to allow elongation
Typically these steps are repeated in a cycle about 30 times generating a large amount of identical DNA copies. Therefore, PCR is often used just before doing an electrophoresis.
The most important part of the PCR reaction is the initial design of the primers. The primers are normally between 18 to 20 base pairs in length and must be completely complimentary to the ends of the DNA region of interest. Included in the PCR reaction must be both the forward and reverse primers, in addition to Taq Polymerase and the DNA template. Alongside these substances the following must also be added; Magnesium Chloride, free nucleotides (dATP, dCTP, dTTP and dGTP) and a Tris-HCl (pH 8.0) buffer.
PCR is carried out in a thermal cycler and the enzyme 'Taq Polymerase' (isolated from Thermus aquaticus) is used as it is thermostable. Originally, DNA polymerase was added to the PCR reaction but it was denatured by the high temperatures, so had to be added at the end of every cycle. However, because Taq polymerase is thermostable, it isn't denatured so only needs to be added at the beginning of the reaction. Pfu (Pyrococcus furiosus) DNA Polymerase can also be used as it has better thermostability than Taq Polymerase and it possesses 3' to 5' proof reading activity.
The technique was developed by Kary Mulis in 1983 for which he was awarded the Nobel Prize in Chemistry in 1993 [3].
When a PCR machine is unavailable a water bath can be used instead.
References
- ↑ Hartl D. L., Ruvolo M. (2012), Genetics: Analysis of genes and genomes, Eight Edition, Jones and Bartlett learning (Chapter 2 DNA Structure and Genetic Variation)
- ↑ Berg, J.M., Tymoczko, J.L. and Stryer, L. (2012). Biochemistry, 7 th Edition, New York , W.H.Freeman &amp; Co Ltd. pg 151
- ↑ http://nobelprize.org/nobel_prizes/chemistry/laureates/1993/mullis-lecture.html