Abstract
We tested the ability of Taq DNA polymerase (Taq) to amplify long DNA fragments and showed that, if the conditions were set properly, Taq could successfully perform the “long PCR” up to 24 kb. The conditions include: (1) longer primers, (2) a 2-step cycling, and (3) a “long buffer.” We propose that the most important requirements are the survival rate of Taq at high temperatures and that of the primers against the 5 to 3 exonuclease activity of Taq.
Keywords: Taq DNA polymerase, long amplicons, primers, reaction buffer
Protein & Peptide Letters
Title: Reevaluating the Capability of Taq DNA Polymerase: Long PCR Amplification
Volume: 14 Issue: 4
Author(s): Hayan Lee, Kyung-Nam Kim and Young Kee Chae
Affiliation:
Keywords: Taq DNA polymerase, long amplicons, primers, reaction buffer
Abstract: We tested the ability of Taq DNA polymerase (Taq) to amplify long DNA fragments and showed that, if the conditions were set properly, Taq could successfully perform the “long PCR” up to 24 kb. The conditions include: (1) longer primers, (2) a 2-step cycling, and (3) a “long buffer.” We propose that the most important requirements are the survival rate of Taq at high temperatures and that of the primers against the 5 to 3 exonuclease activity of Taq.
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Cite this article as:
Lee Hayan, Kim Kyung-Nam and Kee Chae Young, Reevaluating the Capability of Taq DNA Polymerase: Long PCR Amplification, Protein & Peptide Letters 2007; 14 (4) . https://dx.doi.org/10.2174/092986607780363934
DOI https://dx.doi.org/10.2174/092986607780363934 |
Print ISSN 0929-8665 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-5305 |
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