PCR

last authored: March 2010, David LaPierre
last reviewed:

 

 

 

Introduction

PCR, or polymerase chain reaction, is an extremely powerful but very simple technique.

It can turn a very few copies of DNA, from maybe 10 cells, into millions of copies that can then be studied on a gel or by sequencing.

  1. Isolate DNA
  2. pick primers
  3. do PCR
  4. run on a gel
  5. sequence

PCR used to diagnose pathogens will often target structural or housekeeping genes that are not under selective mutational pressure.

 

Explanation of a gel: like running through the bushes with a rope behind you; a short rope will let you move quickly, while a longer ropoe will slow you down.

 

 

 

Uses

 

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Procedure

 

Biotinylated primers can be used. Following amplification, detection can be carried out using streptavidin-chromogen (horseradish peroxidase or alkaline phosphatase.

 

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Resources and References

 

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