Nested polymerase chain reaction

A diagram illustrating the method of nested PCR.

Nested polymerase chain reaction (nested PCR) is a modification of polymerase chain reaction intended to reduce non-specific binding in products due to the amplification of unexpected primer binding sites.[1]

## Polymerase chain reaction[edit]

Polymerase chain reaction itself is the process used to amplify DNA samples, via a temperature-mediated DNA polymerase. The products can be used for sequencing or analysis, and this process is a key part of many genetics research laboratories, along with uses in DNA fingerprinting for forensics and other human genetic cases. Conventional PCR requires primers complementary to the termini of the target DNA. The amount of product from the PCR increases with the number of temperature cycles that the reaction is subjected to. A commonly occurring problem is primers binding to incorrect regions of the DNA, giving unexpected products. This problem becomes more likely with an increased number of cycles of PCR.

## Primers[edit]

Nested polymerase chain reaction involves two sets of primers, used in two successive runs of polymerase chain reaction, the second set intended to amplify a secondary target within the first run product. This allows amplification for a low number of runs in the first round, limiting non-specific products. The second nested primer set should only amplify the intended product from the first round of amplification and not non-specific product. This allows running more total cycles while minimizing non-specific products. This is useful for rare templates or PCR with high background.

## Processes[edit]

The target DNA undergoes the first run of polymerase chain reaction with the first set of primers, shown in green. The selection of alternative and similar primer binding sites gives a selection of products, only one containing the intended sequence.

The product from the first reaction undergoes a second run with the second set of primers, shown in red. It is very unlikely that any of the unwanted PCR products contain binding sites for both the new primers, ensuring the product from the second PCR has little contamination from unwanted products.

## References[edit]

1. ^ Elizabeth van Pelt-Verkuil; Alex van Belkum; John P. Hays (14 March 2008). Principles and Technical Aspects of PCR Amplification. Springer Science & Business Media. pp. 190–. ISBN 978-1-4020-6241-4.

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Polymerase chain reaction techniques

Procedure|

* Initialization
* Cycle
* Denaturation
* Annealing
* Elongation
* Final elongation
* Final hold

Polymerase|

* Klenow
* T4 and T7
* Taq
* Tth
* Pfu
* Vent
* Pwo
* Tli
* Tfu

Optimization
and variants|

* Quantitative polymerase chain reaction (qPCR)
* Reverse transcription polymerase chain reaction (RT-PCR)
* Inverse polymerase chain reaction (inverse PCR)
* Nested polymerase chain reaction (nested PCR)
* Touchdown polymerase chain reaction
* Hot start PCR
* Overlap extension polymerase chain reaction (OE-PCR)
* Multiplex polymerase chain reaction (multiplex PCR)
* Multiplex ligation-dependent probe amplification (MLPA)
* Co-amplification at lower denaturation temperature PCR (COLD-PCR)
* Random amplification of polymorphic DNA (RAPD)

History
and people|

* Kary Mullis
* Kjell Kleppe
* Alice Chien

Portal:

* Biology

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