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The '''selector technique''' is a method to [[polymerase chain reaction|amplify]] and [[Multiplexing|multiplex]] genomic DNA.
The '''selector technique''' allows multiplex amplification of arbitrary sets of genomic sequences. Genomic [[DNA]] is digested with restriction enzymes, circularized by [[hybridisation (molecular biology)|hybridisation]] to selectors and subsequently attached to a vector sequence by [[ligation]]. The procedure results in circular [[DNA]] [[molecules]] with an included general primer pair motif that can be used for amplification by [[PCR]] or RCA.▼
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==Selector construct==
A selector consists of two oligonucleotides, one '''Vector''' oligonucletide and one '''Selector probe'''. Together they form one '''Selector''' with target specific ends on each side of a general primer motif.▼
▲A selector consists of two oligonucleotides, one '''Vector'''
==Selection mechanisms==
==Publications==
*[https://web.archive.org/web/20051127101236/http://nar.oxfordjournals.org/cgi/content/full/33/8/e71 Demonstration of the selector method]▼
*[https://archive.today/20130415163620/http://nar.oxfordjournals.org/cgi/content/full/33/8/e72 The PieceMaker software for designing selector experiments]▼
{{DEFAULTSORT:Selector-Technique}}
▲*[http://nar.oxfordjournals.org/cgi/content/full/33/8/e71 Demonstration of the selector method]
▲*[http://nar.oxfordjournals.org/cgi/content/full/33/8/e72 The PieceMaker software for designing selector experiments]
[[Category:DNA]]
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