U.S. patents available from 1976 to present.
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Method for sequencing nucleic acid molecules

Patent 7033764 Issued on April 25, 2006. Estimated Expiration Date: Icon_subject December 15, 2024. Estimated Expiration Date is calculated based on simple USPTO term provisions. It does not account for terminal disclaimers, term adjustments, failure to pay maintenance fees, or other factors which might affect the term of a patent.

Patent References

Method and structures employing chemically-labelled polynucleotide probes
Patent #: 4994373
Issued on: 02/19/1991
Inventor: Stavrianopoulos, et al.

Nucleic acid hybridization assay employing detectable anti-hybrid antibodies
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Issued on: 04/06/1993
Inventor: Carrico

Method for sequencing polynucleotides
Patent #: 5302509
Issued on: 04/12/1994
Inventor: Cheeseman

Methods and compositions for determining the sequence of nucleic acids
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Method for rapid base sequencing in DNA and RNA with two base labeling
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Automated hybridization/imaging device for fluorescent multiplex DNA sequencing
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Method and apparatus for determining the sequence of polynucleotides
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Method for identifying biochemical and chemical reactions and micromechanical processes using nanomechanical and electronic signal identification
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Methods of preparing probe array by hybridation
Patent #: 5631134
Issued on: 05/20/1997
Inventor: Cantor

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Inventors

Assignee

Application

No. 11014015 filed on 12/15/2004

US Classes:

435/6, Involving nucleic acid435/183, ENZYME (E.G., LIGASES (6. ), ETC.), PROENZYME; COMPOSITIONS THEREOF; PROCESS FOR PREPARING, ACTIVATING, INHIBITING, SEPARATING, OR PURIFYING ENZYMES435/287.2, Measuring or testing for antibody or nucleic acid, or measuring or testing using antibody or nucleic acid436/94, Saccharide (e.g., DNA, etc.)436/164, OPTICAL RESULT536/23.1, DNA or RNA fragments or modified forms thereof (e.g., genes, etc.)536/24.33, Primers536/25.32, Labels or markers utilized (e.g., radiotracer, affinity, fluoroescent, phosphorescent, markers, etc.)536/24.3Probes for detection of specific nucleotide sequences or primers for the synthesis of DNA or RNA

Examiners

Primary: Sisson, Bradley L.

Attorney, Agent or Firm

Foreign Patent References

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International Classes

C12Q 1/68
C12M 3/00
G01N 21/00
C07H 21/02

Abstract

The present invention is directed to a method of sequencing a target nucleic acid molecule having a plurality of bases. In its principle, the temporal order of base additions during the polymerization reaction is measured on a molecule of nucleic acid, i.e. the activity of a nucleic acid polymerizing enzyme on the template nucleic acid molecule to be sequenced is followed in real time. The sequence is deduced by identifying which base is being incorporated into the growing complementary strand of the target nucleic acid by the catalytic activity of the nucleic acid polymerizing enzyme at each step in the sequence of base additions. A polymerase on the target nucleic acid molecule complex is provided in a position suitable to move along the target nucleic acid molecule and extend the oligonucleotide primer at an active site. A plurality of labelled types of nucleotide analogs are provided proximate to the active site, with each distinguishable type of nucleotide analog being complementary to a different nucleotide in the target nucleic acid sequence. The growing nucleic acid strand is extended by using the polymerase to add a nucleotide analog to the nucleic acid strand at the active site, where the nucleotide analog being added is complementary to the nucleotide of the target nucleic acid at the active site. The nucleotide analog added to the oligonucleotide primer as a result of the polymerizing step is identified. The steps of providing labelled nucleotide analogs, polymerizing the growing nucleic acid strand, and identifying the added nucleotide analog are repeated so that the nucleic acid strand is further extended and the sequence of the target nucleic acid is determined.

Other References

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