Molecular Techniques and Methods

Pfu DNA Polymerase

Copy Right © 2001/ Institute of Molecular Development LLC

Pfu DNA polymerase, derived from the hyperthermophilic archae Pyrococcusfuriosus, has been shown to exhibit superior thermostability and proofreading properties compared to other thermostable polymerases. Unlike Taq DNA polymerase, highly thermostable Pfu DNA polymerase possesses 3' to 5' exonuclease proofreading activity that enables the polymerase to correct nucleotide-misincorporation errors. This means that Pfu DNA polymerase-generated PCR fragments will have fewer errors than Taq-generated PCR inserts. Using Pfu DNA polymerase in PCR reactions results in blunt-ended PCR products, which are ideal for cloning into blunt-ended vectors, such as the PCR-Script-vectors. Pfu DNA polymerase is an ideal choice for techniques that require high-fidelity DNA synthesis.




10 x Reaction Buffer
100 mM KCl
100 mM (NH4)2SO4
200 mM Tris-HCl (pH8.7)
20 mM MgSO4
1% Triton X-100
1 mg/ ml BSA




REFERENCES
  • Lundberg, K.S., et al. (1991) Gene 108:1-6.

  • Scott, B, Nielson, K, Cline, J, Kretz, K (1994) Strategies 7: 62-63.

  • Bergseid, M et al. (1991) Strategies 4: 34-35.

  • Cline, I, et al. (1992) Strategies 5: 50.

  • Flanian, JM, et al. (1994) Nucleic Acids Res. 22: 3259-3260.

  • Cline, J, Braman, IC, Hogrefe, HH (1996) Nucleic Acids Res. 24: 3546-3551.



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