In vitro method for producing large amounts of specific
dna or
rna fragments of defined length and sequence from small amounts of short oligonucleotide flanking sequences (primers). The essential steps include thermal denaturation of the double-stranded target molecules, annealing of the primers to their complementary sequences, and extension of the annealed primers by enzymatic synthesis with
dna polymerase. The reaction is efficient, specific, and extremely sensitive. Uses for the reaction include
disease diagnosis, detection of difficult-to-isolate pathogens,
mutation analysis, genetic testing,
dna sequencing, and analyzing evolutionary relationships.
 Instrumentation used in PCR - serc.carleton.edu
|  Polymerase Chain Reaction www.neb.com
|  Polymerase chain reaction en.wikipedia.org
|  Polymerase Chain Reaction (PCR www.accessexcellence.org
|
 For other uses, see PCR en.wikipedia.org
|  With PCR, it is routinely users.rcn.com
|  Time of the PCR experiment bio-ggs.blogspot.com
|  PCR (in vitro DNA www.ucl.ac.uk
|