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PCR Primer Design. http://www.modares.ac.ir/elearning/mnaderi/Genetic%20Engineering%20course%20II/images/2a.jpg. Definition. PCR primer design is the creation of short nucleotide sequences for use in amplifying a specific region of DNA. Examples. PCR primers are designed to:
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PCR Primer Design http://www.modares.ac.ir/elearning/mnaderi/Genetic%20Engineering%20course%20II/images/2a.jpg
Definition • PCR primer design is the creation of short nucleotide sequences for use in amplifying a specific region of DNA.
Examples • PCR primers are designed to: • Highly conserved DNA regions • Protein-coding regions with low degeneracy • More conserved regions that flank variable regions
Non-examples • PCR primers are not designed to: • Repeat regions • Regions with secondary structure • Regions that can form primer-dimers • Regions with low G/C content
Applications • Primer design is used for: • Finding new genes • Developing new identification tools • Optimizing PCRs
Primer Design Criteria • Target: Conserved nucleotide or protein regions • Length: Usually 18 - 24 bases • Purine:pyrimidine content of around 1:1 • End with 1-2 GC pairs, if possible • No inter- or intra-primer interactions • Check with databases for specificity • Cycling conditions and buffer concentrations should be adjusted for each primer pair (see PCR troubleshooting)
Resource http://www.swbic.org/education/bioinfo/pcrprimer.html
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