Choosing primers for qPCR

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Verify by blasting the primers sequences. Target gene should come out with the lowest E value. No other gene should be close. Also check whether possible isoforms will be detected by the candidate primer pair. See also: [[Designing primers]]
Verify by blasting the primers sequences. Target gene should come out with the lowest E value. No other gene should be close. Also check whether possible isoforms will be detected by the candidate primer pair. See also: [[Designing primers]]
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== External links ==
== External links ==
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* [https://www.genscript.com/ssl-bin/app/primer GeneScript TaqMan probe design tool]
* [https://www.genscript.com/ssl-bin/app/primer GeneScript TaqMan probe design tool]
* [http://keck.med.yale.edu/affymetrix/rtpcr/design.htm TaqMan design tips using Primer Express], Yale (note Primer Express is commercial software [[Image:padlock-closed.png]] single license <8000€)
* [http://keck.med.yale.edu/affymetrix/rtpcr/design.htm TaqMan design tips using Primer Express], Yale (note Primer Express is commercial software [[Image:padlock-closed.png]] single license <8000€)
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* [http://www.protocol-online.org/prot/Research_Tools/Online_Tools/Oligo_Design/Real-Time_PCR_Primer/ more links from protocol-online.org]
* [http://www.protocol-online.org/prot/Research_Tools/Online_Tools/Oligo_Design/Real-Time_PCR_Primer/ more links from protocol-online.org]
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* [http://www.hsls.pitt.edu/guides/genetics/obrc/dna/pcr_oligos qPCR link list] from Health Science Library, Uni Pittsburgh

Revision as of 12:03, 5 March 2008

What are the best primers for my qPCR experiment? Choosing suitable primers is an early crucial step in your quantitative reverse transcriptase PCR experiment - QRT-PCR. Reusing a tested primer pair from a repository or publication can save you some time. Otherwise primer selection from scratch is similar to that for a standard qualitative PCR experiment with some small variations.

Primer repositories and collections

Primer databases can help you save the time of designing and testing your own primers. It is also intended to facilitate standardisation among different laboratories.

  • RTPrimerDB is a collection of user submitted qPCR primers and probe sequences mostly human (2835), mouse (624), and rat (388) based on stats from 2/08. The database includes SYBR Green I, Taqman, Hybridisation Probes, and Molecular Beacon. Other features include: mfold secondary structure prediction, primer alignment, and BLAST. The database is hosted by the Center for Medical Genetics, Gent, Belgium. Please submit you tested primer pairs. Publication describing the database [PMID 16381959].
  • PrimerBank is a public database for human and mouse qRT-PCR primers. PrimerBank contains over 306,800 primers covering most (percentage??) known human and mouse genes. The creators of the repository report that 26,855 primer pairs tested corresponding to 27,681 mouse genes had a design success rate of 82.6% (22,187 successful primer pairs) based on agarose gel electrophoresis. Don't neglect to check the efficiency and specificity of the oligos yourself though. Primers are designed to have a Tm of 60-63°C and a product of 100-250nt [1]. Link to paper.
  • qPrimerDepot is a public database for human qRT-PCR primers searchable with either RefSeq ID or HUGO gene name. It claims to contain 99% of human RefSeq sequences. For 99% of intron-bearing genes, the PCR product will cross an exon-exon border which overlaps one of the largest introns. All primers have annealing temperatures of approximately 60°C. Link to paper.

Primer design

An excellent and fast way to select primers is with the free online-tool Primer3, currently in v0.3. Primer3Plus, a variation of Primer3 has qPCR settings. Or just apply the following or similar settings to Primer3:

  • pair towards 3' end (often more specific, some cDNAs don't contain)
  • pair separated by an exon-exon boundary (reduces genomic background) e.g. last exon & penultimate
  • amplified region must be no biger than 200 bp; usally 60-150 bp
  • GC content: 50-60%
  • min length: 18, max length 24 (best: 20 nt)
  • melting temperature: min 60, max 63, best 60
  • max Tm difference: 10 (shouldn't be more than 1 in final pair)
  • max 3' self complementary: 1
  • max poly-x: 3

Verify by blasting the primers sequences. Target gene should come out with the lowest E value. No other gene should be close. Also check whether possible isoforms will be detected by the candidate primer pair. See also: Designing primers

External links

Personal tools