Dual asymmetric PCR: One-step construction of synthetic genes

G. S. Sandhu, R. A. Aleff, B. C. Kline

Research output: Contribution to journalArticle

58 Citations (Scopus)

Abstract

We have developed a one-step process for constructing synthetic genes. Four adjacent oligonucleotides 17-100 bases in length having short overlaps of 15-17 bases are used as primers in a PCR mixture. The quantity of the two internal primers is highly limited, and the resultant reaction causes an asymmetric single-stranded amplification of the two halves of the total sequence due to an excess of the two flanking primers. In subsequent PCR cycles, these dual asymmetrically amplified fragments, which overlap each other, yield a double-stranded, full-length product.

Original languageEnglish (US)
JournalBioTechniques
Volume12
Issue number1
StatePublished - 1992

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Synthetic Genes
Oligonucleotides
Amplification
Genes
Polymerase Chain Reaction

ASJC Scopus subject areas

  • Biochemistry, Genetics and Molecular Biology(all)
  • Clinical Biochemistry

Cite this

Sandhu, G. S., Aleff, R. A., & Kline, B. C. (1992). Dual asymmetric PCR: One-step construction of synthetic genes. BioTechniques, 12(1).

Dual asymmetric PCR : One-step construction of synthetic genes. / Sandhu, G. S.; Aleff, R. A.; Kline, B. C.

In: BioTechniques, Vol. 12, No. 1, 1992.

Research output: Contribution to journalArticle

Sandhu, GS, Aleff, RA & Kline, BC 1992, 'Dual asymmetric PCR: One-step construction of synthetic genes', BioTechniques, vol. 12, no. 1.
Sandhu, G. S. ; Aleff, R. A. ; Kline, B. C. / Dual asymmetric PCR : One-step construction of synthetic genes. In: BioTechniques. 1992 ; Vol. 12, No. 1.
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