The selector technique is a method to amplify and multiplex genomic DNA.

Process

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Genomic DNA is digested with restriction enzymes, circularized by 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.

Selector construct

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A selector consists of two oligonucleotides, one Vector oligonucleotide and one Selector probe. Together they form one Selector with _target specific ends on each side of a general primer motif.

Selection mechanisms

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  1. A selector probe hybridizes with both ends of the selected _target.
  2. A selector probe hybridizes with one end to the 3’ end of the _target and the other end to an internal sequence of the _target. The protruding 5' end is cleaved off using Taq polymerase.

Publications

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