Chemistry: molecular biology and microbiology – Micro-organism – tissue cell culture or enzyme using process... – Preparing compound containing saccharide radical
Patent
1996-05-08
1999-11-16
Fredman, Jeffrey
Chemistry: molecular biology and microbiology
Micro-organism, tissue cell culture or enzyme using process...
Preparing compound containing saccharide radical
435 6, 536 243, 536 2431, 536 2432, 536 2433, C12P 1934, C12Q 168, C07H 2102
Patent
active
059856190
ABSTRACT:
The present invention provides admixtures and methods for PCR amplification of a target nucleic acid in which amplification efficiency is increased by including an antibody specific for a polymerization agent and at least one of an exonuclease and a glycosylase in the PCR reaction mix. Kits for amplification of a target nucleic acid are also provided.
REFERENCES:
patent: 5273890 (1993-12-01), Steinman
patent: 5418149 (1995-05-01), Gelfand
patent: 5605796 (1997-02-01), Chen et al.
Sharkey, et al.: "Antibodies as Thermolabile Switches: High Temperature Triggering for the Polymerase Chain Reaction", Biotechnology, vol. 12, May 1994, New York, U.S. pp. 506-509.
Longo, et al.: "Use of Uracil DNA Glycosylase to Control Carry-Over Contamination in Polymerase Chain Reactions", Gene, vol. 93, No. 1, Jan. 1990, Amsterdam, NL pp. 125-128.
Li et al.: "Eliminating Primers from Completed Polymerase Chain Reactions with Exonuclease VII", Nucleic Acids Research, vol. 19, No. 11, Jun. 11, 1991, Oxford, GB, pp. 3139-3141.
Zhu, et al.: "The Use of Exonuclease III for Polymerase Chain Reaction Sterilization", Nucleic Acids Research, vol. 19, No. 9, May 11, 1991, Oxford, GB, p. 2511.
Findlay et al, (1993), "Automated closed-vessel system for in vitro diagnostics based on polymerase chain reaction", Clin. Chem. 39(9):1927-1933.
Longo et al, (1990), "Use of uracil DNA glycosylase to control carryover contamination in polymerase chain reactions" Gene 93:124-128.
Stratagene catalog, (1988), p. 39.
Hanke et al, (May 1994), "Direct DNA sequencing of PCR-amplified vector inserts following enzymatic degradation of primer and dNTPs" Biotechniques 17(5):858-860.
Ott et al, (1987), "Protection of oligonucleotide primers against degradation by DNA polymerase I", Biochemistry 26:8237-8241.
Scalice et al, (1994), "Monoclonal antibodies prepared against the DNA polymerase from Thermus aquaticus are potent inhibitors of enzyme activity", J. Imm. Meth. 172:147-163.
Kellog et al, (1994), "TaqStart antibody.TM.: Hot Start PCR facilitated by a neutralizing monoclonal antibody directed against Taq DNA polymerase", Biotechniques 16(6):1134-1137.
Kox et al, (Mar. 1994), "A more reliable PCR for detection of Mycobacterium tuberculosis in clinical samples", J. Clin. Microbiol. 32(3):672-678.
Sharkey et al (May 1994), "Antibodies as thermolabile switches: high temperature in clinical samples", J. Clin. Microbiol. 32(3):672-678.
Scalice et al, (1993), "The use of Mg + 2 encapsulation or TAQ DNA polymerase inhibiting antibodies to prevent o-cycle artifacts in the polymerase chain reaction", Clin. Chem. 39(6):1180.
Stratagene catalog, p. 196, 1995.
Promega catalog, p. 55, 1993.
Patterson David Robert
Sutherland John William Henderson
Clinical Diagnostic Systems, Inc.
Fredman Jeffrey
LandOfFree
Use of exonuclease and/or glycosylase as supplements to anti-pol does not yet have a rating. At this time, there are no reviews or comments for this patent.
If you have personal experience with Use of exonuclease and/or glycosylase as supplements to anti-pol, we encourage you to share that experience with our LandOfFree.com community. Your opinion is very important and Use of exonuclease and/or glycosylase as supplements to anti-pol will most certainly appreciate the feedback.
Profile ID: LFUS-PAI-O-1323355