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PCR

An in vitro technique that can rapidly amplify a target DNA sequence

Template DNA

Double-stranded DNA that contains the target sequence to be amplified

PCR Steps

Denaturation


Annealing


Extension

3

Denaturation

PCR is heated to 94c


The heat denatures the double-stranded DNA

Annealing

PCR mix is cooled to 55c


Allow primers to anneal to each template strand


Primers flank the target sequence to be amplified

Extension

PCR mix is heated to 72c


Taq polymerase synthesizes a strand of DNA complementary to the template strands


Extending from the 3' end of the primers

Transporter gene

Gene determining eye color

Magnesium use

Allows the Taq polymerase to bind

dNTP use

Building blocks that base pair the new strand via Taq polymerase


(N=A, C, G, T)

*Primers use (P1, P2, P3)

Tells where to start DNA replication

Taq polymerase

Enzyme that creates DNA