IP Library Granted Patent US 7,312,039
Granted Patent B2
US 7,312,039 · App. 11/590,056 · Granted Dec 25, 2007

Detection of nucleic acid sequence differences using coupled ligase detection and polymerase chain reactions

Assignees: Cornell Research Foundation, Inc.; Regents of the University of Minnesota; Board of Supervisors of Louisiana State University and Agricultural and Mechanical College
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Quick Facts
Patent No.
US 7,312,039
App. No.
11/590,056
Granted
Dec 25, 2007
Kind
B2
Abstract

The present invention relates to a method for identifying a target nucleotide sequence. This method involves forming a ligation product on a target nucleotide sequence in a ligase detection reaction mixture, amplifying the ligation product to form an amplified ligation product in a polymerase chain reaction (PCR) mixture, detecting the amplified ligation product, and identifying the target nucleotide sequence. Such coupling of the ligase detection reaction and the polymerase chain reaction permits multiplex detection of nucleic acid sequence differences.

Claims (9)

1. A method for identifying a target nucleotide sequence comprising:

forming a ligation product on a target nucleotide sequence in a ligation detection reaction mixture, wherein the ligation product comprises an upstream primer portion and a downstream primer portion, wherein the upstream primer portion and the downstream primer portion are not complementary with the target nucleotide sequence;

amplifying the ligation product to form an amplified ligation product in a polymerase chain reaction (PCR) mixture, wherein the PCR mixture comprises an upstream primer and a downstream primer; and

detecting the amplified ligation product to identify the target nucleotide sequence.

2. The method according to claim 1 wherein the ligation detection reaction mixture comprises adjacently hybridizing ligation probes.

3. The method according to claim 1 wherein the ligation product results from the ligation of two ligation probes, wherein the two ligation probes are two different molecules.

4. The method according to claim 1 , wherein the upstream primer or the downstream primer contains a label.

5. The method according to claim 1 , wherein the ligation product can be distinguished from other nucleic acids in the PCR, said method further comprising:

providing a solid support with different capture oligonucleotides immobilized at different particular sites, wherein the capture oligonucleotides have nucleotide sequences complementary to a unique nucleotide sequence of an extension product.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 16, 2009
From: BOARD OF SUPERVISORS OF LOUISIANA STATE UNIVERSITY AND AGRICULTURAL AND MECHANICAL COLLEGE; REGENTS OF THE UNIVERSITY OF MINNESOTA
To: CORNELL RESEARCH FOUNDATION, INC.
Reel/Frame 023660/0322 →
CONFIRMATORY LICENSE Recorded Feb 4, 2009
From: CORNELL UNIVERSITY
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 022200/0792 →
Continuity (7)
Continuation 1122936600 · Sep 16, 2005
Continuation 1084372000 · May 12, 2004
Continuation 0991815600 · Jul 30, 2001
Continuation 0944052300 · Nov 15, 1999
Division 0886447300 · May 28, 1997
Provisional Application 6001853200 · May 29, 1996
Related Publication 20070048783A1 · Mar 1, 2007