期刊
NUCLEIC ACIDS RESEARCH
卷 33, 期 16, 页码 5219-5225出版社
OXFORD UNIV PRESS
DOI: 10.1093/nar/gki840
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资金
- NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES [R01GM067986, R01GM053936] Funding Source: NIH RePORTER
- NIGMS NIH HHS [GM067986, GM053936, R01 GM067986, R01 GM053936] Funding Source: Medline
Therminator DNA polymerase is an efficient DNA-dependent TNA polymerase capable of polymerizing TNA oligomers of at least 80 nt in length. In order for Therminator to be useful for the in vitro selection of functional TNA sequences, its TNA synthesis fidelity must be high enough to preserve successful sequences. We used sequencing to examine the fidelity of Therminator-catalyzed TNA synthesis at different temperatures, incubation times, tNTP ratios and primer/template combinations. TNA synthesis by Therminator exhibits high fidelity under optimal conditions; the observed fidelity is sufficient to allow in vitro selection with TNA libraries of at least 200 nt in length.
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