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:
Jun. 26, 2018

Filed:

May. 19, 2017
Applicant:

Gen-probe Incorporated, San Diego, CA (US);

Inventors:

Gary D. Lair, San Diego, CA (US);

Thanh N. Nguyen, Laguna Niguel, CA (US);

Haitao Li, San Diego, CA (US);

Florence Li, San Diego, CA (US);

Byron J. Knight, San Diego, CA (US);

Robert E. Heinz, San Diego, CA (US);

Jerzy A. Macioszek, Chevy Chase, MD (US);

Christopher B. Davis, San Diego, CA (US);

Robert F. Scalese, Carlsbad, CA (US);

Assignee:

GEN-PROBE INCORPORATED, San Diego, CA (US);

Attorneys:
Primary Examiner:
Int. Cl.
CPC ...
B01L 3/00 (2006.01); G01N 21/00 (2006.01); G01N 21/64 (2006.01); G01N 35/00 (2006.01); G01N 35/02 (2006.01); G01N 35/04 (2006.01); G01N 35/10 (2006.01); G01N 21/76 (2006.01); C12Q 1/6851 (2018.01);
U.S. Cl.
CPC ...
G01N 21/6428 (2013.01); C12Q 1/6851 (2013.01); G01N 21/76 (2013.01); G01N 35/0092 (2013.01); G01N 35/0098 (2013.01); G01N 35/0099 (2013.01); G01N 35/025 (2013.01); G01N 35/026 (2013.01); G01N 35/04 (2013.01); G01N 35/1002 (2013.01); G01N 2021/6419 (2013.01); G01N 2021/6421 (2013.01); G01N 2021/6432 (2013.01); G01N 2021/6439 (2013.01); G01N 2035/0097 (2013.01); G01N 2035/00356 (2013.01); G01N 2035/00524 (2013.01); G01N 2035/0441 (2013.01); G01N 2035/0443 (2013.01); G01N 2035/0444 (2013.01); G01N 2035/0455 (2013.01); G01N 2035/0491 (2013.01);
Abstract

A continuous process for performing multiple nucleic acid amplification assays, where at least a portion of a second subset of reaction mixtures are transferred to a heater while a first subset of reaction mixtures are being subjected to conditions for performing a nucleic acid amplification assay. During the process, a plurality of reaction mixtures from the first and second subsets of reaction mixtures are simultaneously subjected to conditions sufficient to perform multiple nucleic acid amplification assays in the reaction mixtures. The presence or absence of a target nucleic acid in the first subset of reaction mixtures is determined while the reaction mixtures are in the heater.


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