Method of amplification of one or more DNA sequences in a...

Chemistry: molecular biology and microbiology – Measuring or testing process involving enzymes or... – Involving nucleic acid

Reexamination Certificate

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C435S091200

Reexamination Certificate

active

06936420

ABSTRACT:
A method of amplification of one or more DNA sequences in a DNA containing sample, and methods of investigating such samples are provided in which an improved amplification cycling regime is used. The regime features a first phase and a second phase, the first phase including a denaturation temperature step, followed by an annealing temperature step, followed by a corrected annealed primer extension temperature step, these steps being followed by an annealing temperature step, corrected annealed primer extension temperature step prior to any further denaturation temperature steps being applied. Increased amplification from a given number of amplification cycles and maximised sensitivity for the DNA amplification process is achieved as a result.

REFERENCES:
patent: 5705366 (1998-01-01), Backus
patent: 6040166 (2000-03-01), Erlich et al.
patent: 0 648 845 (1995-04-01), None
patent: 0 694 617 (1996-01-01), None
patent: 01/07640 (2001-02-01), None
Wu et al., “The Effect of Temperature and Oligonucleotide Primer Length on the Specificity and Efficiency of Amplification by the Polymerase Chain Reaction”, DNA and Cell Biology, vol. 10, No. 3, pp. 233-238, Apr. 1991.
Sugimoto et al., “Quanatative Detection of DNA by Coamplification Polymerase Chain Reaction: A wide Detectable Range Controlled by the Thermodynamic Stability of Primer Template Duplexes”, Analytical Biochemistry, vol. 211, No. 1, pp. 170-172, May 1993.
Backus et al., “Method of Amplification Using Intermediate Renaturation Step”, Biotechnology Advances Research Reviews and Patent Abstracts vol. 15 No. 2, 1997 Abstract.

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