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Nucleic Acids Res. 1989 July 11; 17(13): 5408.
PMCID: PMC318147

The use of native T7 DNA polymerase for site-directed mutagenesis.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.
  • Craik CS, Largman C, Fletcher T, Roczniak S, Barr PJ, Fletterick R, Rutter WJ. Redesigning trypsin: alteration of substrate specificity. Science. 1985 Apr 19;228(4697):291–297. [PubMed]
  • Masamune Y, Richardson CC. Strand displacement during deoxyribonucleic acid synthesis at single strand breaks. J Biol Chem. 1971 Apr 25;246(8):2692–2701. [PubMed]
  • Nossal NG. DNA synthesis on a double-stranded DNA template by the T4 bacteriophage DNA polymerase and the T4 gene 32 DNA unwinding protein. J Biol Chem. 1974 Sep 10;249(17):5668–5676. [PubMed]
  • Huang CC, Hearst JE, Alberts BM. Two types of replication proteins increase the rate at which T4 DNA polymerase traverses the helical regions in a single-stranded DNA template. J Biol Chem. 1981 Apr 25;256(8):4087–4094. [PubMed]
  • Lechner RL, Engler MJ, Richardson CC. Characterization of strand displacement synthesis catalyzed by bacteriophage T7 DNA polymerase. J Biol Chem. 1983 Sep 25;258(18):11174–11184. [PubMed]
  • Tabor S, Huber HE, Richardson CC. Escherichia coli thioredoxin confers processivity on the DNA polymerase activity of the gene 5 protein of bacteriophage T7. J Biol Chem. 1987 Nov 25;262(33):16212–16223. [PubMed]

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