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

Nucleic acid probe, test kit and diagnostic and purification methods

Patent 5328825 Issued on July 12, 1994. Estimated Expiration Date: Icon_subject March 6, 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

Fine carrier particles sensitized with acylated antibody for antigen detection
Patent #: 4591571
Issued on: 05/27/1986
Inventor: Kuboyama ,   et al.

Process for amplifying, detecting, and/or-cloning nucleic acid sequences
Patent #: 4683195
Issued on: 07/28/1987
Inventor: Mullis ,   et al.

Coupling of nucleic acids to solid support by photochemical methods
Patent #: 4713326
Issued on: 12/15/1987
Inventor: Dattagupta ,   et al.

Polynucleotide determination with selectable cleavage sites
Patent #: 4775619
Issued on: 10/04/1988
Inventor: Urdea

Immunoreactive reagent particles having tracer, receptor molecules and protein of pI less than 6
Patent #: 4812414
Issued on: 03/14/1989
Inventor: Warren, III ,   et al.

Agglutination reagent and method of preparing same Patent #: 4828978
Issued on: 05/09/1989
Inventor: Warren, III ,   et al.

Inventors

Application

No. 847447 filed on 03/06/1992

US Classes:

435/6, Involving nucleic acid435/5, Involving virus or bacteriophage435/91.2, Acellular exponential or geometric amplification (e.g., PCR, etc.)536/24.3Probes for detection of specific nucleotide sequences or primers for the synthesis of DNA or RNA

Examiners

Primary: Parr, Margaret
Assistant: Myers, Carla J.

Attorney, Agent or Firm

Foreign Patent References

  • 70687 EP. 01/13/1983
  • 8801302 WO. 02/13/1988

International Classes

C12Q 001/68
C07H 021/04

Abstract

An oligonucleotide is linked to a particle through a protein or carbohydrate to form a water-insoluble nucleic acid probe. The protein or carbohydrate has a pI of about 6 or less, and has been chemically modified with an acylating, alkylating or sulfonylating agent. The particle surface is substantially free of other proteins or carbohydrates. The probe is useful in various diagnostic and purification methods wherein hybridization of the oligonucleotide with a target nucleic acid is possible. In one instance, the probe can be used to capture a DNA strand which has been amplified using polymerase chain reaction techniques.

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