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Nucleic Acids Res. Aug 25, 1992; 20(16): 4371.
PMCID: PMC334154

Minimizing deletion mutagenesis artifact during Taq DNA polymerase PCR by E. coli SSB.


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Selected References

These references are in PubMed. This may not be the complete list of references from this article.
  • Cariello NF, Thilly WG, Swenberg JA, Skopek TR. Deletion mutagenesis during polymerase chain reaction: dependence on DNA polymerase. Gene. 1991 Mar 1;99(1):105–108. [PubMed]
  • Pallansch L, Beswick H, Talian J, Zelenka P. Use of an RNA folding algorithm to choose regions for amplification by the polymerase chain reaction. Anal Biochem. 1990 Feb 15;185(1):57–62. [PubMed]
  • Chou Q, Russell M, Birch DE, Raymond J, Bloch W. Prevention of pre-PCR mis-priming and primer dimerization improves low-copy-number amplifications. Nucleic Acids Res. 1992 Apr 11;20(7):1717–1723. [PMC free article] [PubMed]
  • Green IR, Sargan DR. Sequence of the cDNA encoding ovine tumor necrosis factor-alpha: problems with cloning by inverse PCR. Gene. 1991 Dec 30;109(2):203–210. [PubMed]
  • Tabor S, Richardson CC. DNA sequence analysis with a modified bacteriophage T7 DNA polymerase. Proc Natl Acad Sci U S A. 1987 Jul;84(14):4767–4771. [PMC free article] [PubMed]

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