Sequencing of Double-Stranded PCR Products

Research output: Contribution to journalArticle

Abstract

Very often the experimental step following PCR is sequencing of the amplified fragment. Two protocols that allow direct sequencing of a double-stranded PCR product are described. The first involves removal of one strand of the PCR product using an M13 single-stranded DNA clone, allowing the second strand to be sequenced. The second protocol involves Maxam-Gilbert chemical sequencing after PCR amplification with one labeled primer. The advantages and disadvantages of the two protocols are compared, but both yield DNA sequence without cloning of the PCR product.

Original languageEnglish (US)
Pages (from-to)159-164
Number of pages6
JournalApplied Biochemistry and Biotechnology - Part B Molecular Biotechnology
Volume5
Issue number2
DOIs
StatePublished - Jan 1 1996

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Cloning
Single-Stranded DNA
DNA sequences
Amplification
DNA
Polymerase Chain Reaction
Organism Cloning
Clone Cells

All Science Journal Classification (ASJC) codes

  • Biotechnology
  • Bioengineering
  • Biochemistry
  • Applied Microbiology and Biotechnology
  • Molecular Biology

Cite this

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Sequencing of Double-Stranded PCR Products. / Gal, Susannah.

In: Applied Biochemistry and Biotechnology - Part B Molecular Biotechnology, Vol. 5, No. 2, 01.01.1996, p. 159-164.

Research output: Contribution to journalArticle

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