The patent badge is an abbreviated version of the USPTO patent document. The patent badge does contain a link to the full patent document.

The patent badge is an abbreviated version of the USPTO patent document. The patent badge covers the following: Patent number, Date patent was issued, Date patent was filed, Title of the patent, Applicant, Inventor, Assignee, Attorney firm, Primary examiner, Assistant examiner, CPCs, and Abstract. The patent badge does contain a link to the full patent document (in Adobe Acrobat format, aka pdf). To download or print any patent click here.

Date of Patent:
Dec. 22, 2009

Filed:

Jul. 08, 2005
Applicants:

Ronald M. Cook, Novato, CA (US);

Eliana Saxon Armstrong, Richmond, CA (US);

Hans E. Johansson, El Cerrito, CA (US);

Inventors:

Ronald M. Cook, Novato, CA (US);

Eliana Saxon Armstrong, Richmond, CA (US);

Hans E. Johansson, El Cerrito, CA (US);

Assignee:

Biosearch Technologies, Inc., Novato, CA (US);

Attorney:
Primary Examiner:
Int. Cl.
CPC ...
G01N 33/533 (2006.01); G01N 33/53 (2006.01); C12Q 1/26 (2006.01); C12N 1/21 (2006.01); C12P 21/00 (2006.01);
U.S. Cl.
CPC ...
Abstract

In one aspect, the invention provides fluorescent probes and assays. The probes include a fluorophore-quencher pair that undergoes a switch from dark to fluorescent in response to a reaction of the quencher. The switch of the probe from dark to fluorescent is typically mediated by an enzyme that acts directly or indirectly on the quencher, interfering with its ability to quench fluorescence emission from the fluorophore. In another aspect, the invention provides a reporter gene assay system and methods of using this system. The assay system includes a fluorophore-quencher probe and an enzyme that acts directly or indirectly on the quencher, increasing the fluorescent emission of the fluorophore. In still other aspects, the invention provides nucleic acid constructs and cells expressing the peptide products of these constructs. In assays of the invention, the presence of a target substance is detected by the switching of fluorescence mediated by the change in oxidation state of the quencher. The assay systems are of use in numerous assay formats, e.g., confirming the expression of the enzyme that acts on the quencher, and/or detecting a species conjugated to the enzyme.


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