IP Library › Granted Patent US 8,198,026
Granted Patent B2
US 8,198,026 · App. 11/553,223 · Granted Jun 12, 2012

Method of detecting specific fragments of DNA or RNA with the aid of a real-time polymerase chain reaction

Assignee: Institut Biokhimii I Genetiki Ufimskogo Nauchnogo Tsentra Ran
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Quick Facts
Patent No.
US 8,198,026
App. No.
11/553,223
Granted
Jun 12, 2012
Kind
B2
Abstract

Methods of amplifying specific fragments of DNA or RNA with the aid of a polymerase chain reaction in real time are disclosed. The methods include providing a first oligonucleotide primer that comprises a donor fluorescent dye and a second oligonucleotide primer that comprises an acceptor fluorescent dye; allowing the primers to anneal to a target nucleic acid at positions abutting to each other or overlapping; carrying out a polymerase chain reaction which allows for a fluorescent resonance transfer of energy between the donor dye and the acceptor dye; detecting an increase of fluorescent emission of the acceptor dye; and correlating the increase in the emission of the acceptor dye with the accumulation of the specific fragment of DNA or RNA. In one embodiment, the primers comprise a fluorescent dye and a universal quencher.

Claims (14)

1. A method of amplifying specific fragments of a target DNA or RNA with the aid of a polymerase chain reaction in real time, the method comprising:

(a) providing a first oligonucleotide primer that comprises a donor fluorescent dye and a second oligonucleotide primer that comprises an acceptor fluorescent dye, wherein the first and second oligonucleotide primers are designed to anneal to partially overlapping portions of a target nucleic acid, wherein such overlap is not more than one nucleotide;

(b) allowing the primers to anneal to the target nucleic acid at partially overlapping positions;

(c) carrying out a polymerase chain reaction which allows for a fluorescent resonance transfer of energy between the donor dye and the acceptor dye;

(d) detecting an increase of fluorescent emission of the acceptor dye; and

(e) correlating the increase in the emission of the acceptor dye with the accumulation of the specific fragment of DNA or RNA.

2. The method of claim 1 , wherein the first oligonucleotide primer is a forward primer, and the second oligonucleotide primer is a reverse primer.

3. A method of amplifying specific fragments of a target DNA or RNA with the aid of a polymerase chain reaction in real time, the method comprising:

(a) providing a first oligonucleotide primer that comprises a fluorescent dye and a second oligonucleotide primer that comprises a universal quencher, wherein the first and second oligonucleotide primers are designed to anneal to partially overlapping portions of a target nucleic acid, wherein such overlap is not more than one nucleotide;

(b) allowing the primers to anneal to the target nucleic acid at partially overlapping positions;

(c) carrying out a polymerase chain reaction which allows for a quenching effect between the fluorescent dye and the universal quencher;

(d) detecting a reduction in emission of the fluorescent dye; and

(e) correlating the decrease in the emission of the fluorescent dye with the accumulation of the specific fragment of DNA or RNA.

4. The method of claim 3 , wherein the first oligonucleotide primer is a forward primer, and the second oligonucleotide primer is a reverse primer.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 31, 2007
From: CHEMERIS, ALEXEI VIKTOROVICH; NIKONOROV, YURY MIKHAILOVICH; ROMANENKOVA, MAIYA LEONIDOVNA; CHEMERIS, DMITRY ALEXEEVICH; GARAFUTDINOV, RAVIL RINATOVICH; MAGAZOVA, ROZA AZATOVNA; MALEEV, GRIGORY VLADIMIROVICH; VAKHITOV, VENER ABSATAROVICH; VASILOV, RAIF GAYANOVICH
To: INSTITUT BIOKHIMII I GENETIKI UFIMSKOGO
Reel/Frame 018835/0665 →
Priority Claims (1)
RU 2005132940 · Oct 26, 2005 · national
Continuity (1)
Related Publication 20070117125A1 · May 24, 2007