U.S. patents available from 1976 to present.
U.S. patent applications available from 2005 to present.

Nucleic acid assay method

Patent 5242797 Issued on September 7, 1993. Estimated Expiration Date: Icon_subject January 2, 2012. 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

3652761

Test article including a covalently attached diagnostic reagent and method
Patent #: 4133639
Issued on: 01/09/1979
Inventor: Harte

Fluorescent immunoassay employing optical fiber in capillary tube
Patent #: 4447546
Issued on: 05/08/1984
Inventor: Hirschfeld

Nucleic acid hybridization assay employing antibodies to intercalation complexes
Patent #: 4563417
Issued on: 01/07/1986
Inventor: Albarella ,   et al.

Immediate ligand detection assay
Patent #: 4568649
Issued on: 02/04/1986
Inventor: Bertoglio-Matte

Process for labeling nucleic acids using psoralen derivatives
Patent #: 4582789
Issued on: 04/15/1986
Inventor: Sheldon, III ,   et al.

Immunoassay apparatus
Patent #: 4671938
Issued on: 06/09/1987
Inventor: Cook

Selective zeolitic adsorbent and a method for activation thereof
Patent #: 4713362
Issued on: 12/15/1987
Inventor: Maroulis ,   et al.

Use of non-hybridizable nucleic acids for the detection of nucleic acid hybridization Patent #: 4724202
Issued on: 02/09/1988
Inventor: Dattagupta ,   et al.

Inventor

Assignee

Application

No. 817942 filed on 01/02/1992

US Classes:

435/6, Involving nucleic acid435/5, Involving virus or bacteriophage436/63, BIOLOGICAL CELLULAR MATERIAL TESTED436/94Saccharide (e.g., DNA, etc.)

Examiners

Primary: Chambers, Scott A.

Foreign Patent References

  • 0070687 EP. 01/13/1983
  • 0131830 EP. 01/13/1985
  • 2139349 GB. 11/13/1984

International Classes

C12Q 001/68
C12Q 001/70
G01N 033/00
G01N 033/48

Abstract

An assay for polynucleotides employing total internal reflection of excitation radiation at a coating bonded to the surface of an optically conductive glass cell. The coating initially includes single-stranded polynucleotides coupled to individual attachment sites on the surface of the cell, such polynucleotides being complementary, at least in part to the single-stranded form of the polynucleotide that is being assayed. Each molecule of the coupled polynucleotide is connected to the cell surface through a spacer connected to an irreversibly conjugated polyadenine/polythymidine sequence at one end of the coupled polynucleotide.When the surface of the coated cell is contacted with a sample that contains single-stranded polynucleotide complementary to the bound polynucleotide, renaturation will occur, forming a double-stranded form of the polynucleotide of interest. A fluorochrome dye specific to that double-stranded form is coupled to the latter, the dye including a chromophore that the excitation radiation will excite into fluorescence. The induced fluorescence is then gathered and measured.

Other References

  • Dilica, K. Understanding DNA and Gene Cloning; John Wiley & Sons N.Y. 1984 p. 12
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