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:
Mar. 21, 2017

Filed:

Oct. 17, 2007
Applicants:

Kelly G. Ammann, Longmont, CO (US);

Ralph E. Burns, Boulder, CO (US);

Ernest V. Hansberry, Evergreen, CO (US);

Glenn A. Horner, Boulder, CO (US);

Cheryl A. Jakub, Golden, CO (US);

John E. Kling, San Diego, CA (US);

Donald J. Nieglos, Superior, CO (US);

Robert E. Schneider, Erie, CO (US);

Robert J. Smith, Louisville, CO (US);

Inventors:

Kelly G. Ammann, Longmont, CO (US);

Ralph E. Burns, Boulder, CO (US);

Ernest V. Hansberry, Evergreen, CO (US);

Glenn A. Horner, Boulder, CO (US);

Cheryl A. Jakub, Golden, CO (US);

John E. Kling, San Diego, CA (US);

Donald J. Nieglos, Superior, CO (US);

Robert E. Schneider, Erie, CO (US);

Robert J. Smith, Louisville, CO (US);

Assignee:

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

Attorneys:
Primary Examiner:
Assistant Examiner:
Int. Cl.
CPC ...
C12M 1/34 (2006.01); C12M 1/40 (2006.01); C12Q 1/68 (2006.01); B01F 9/00 (2006.01); B01L 7/00 (2006.01); B03C 1/28 (2006.01); B03C 1/30 (2006.01); G01N 35/02 (2006.01); B01L 9/06 (2006.01); G01N 35/00 (2006.01); G01N 35/10 (2006.01); G01N 35/04 (2006.01);
U.S. Cl.
CPC ...
C12Q 1/6834 (2013.01); B01F 9/0001 (2013.01); B01F 9/0014 (2013.01); B01F 9/0021 (2013.01); B01L 7/52 (2013.01); B01L 7/5255 (2013.01); B03C 1/282 (2013.01); B03C 1/288 (2013.01); B03C 1/30 (2013.01); C12Q 1/6813 (2013.01); C12Q 1/6832 (2013.01); G01N 35/025 (2013.01); B01F 2009/0074 (2013.01); B01L 9/06 (2013.01); B01L 2200/147 (2013.01); B01L 2300/1822 (2013.01); B01L 2300/1827 (2013.01); B03C 2201/26 (2013.01); C12Q 2537/10 (2013.01); G01N 35/0098 (2013.01); G01N 35/0099 (2013.01); G01N 35/1065 (2013.01); G01N 2035/00356 (2013.01); G01N 2035/00524 (2013.01); G01N 2035/0437 (2013.01); G01N 2035/0455 (2013.01); G01N 2035/103 (2013.01); Y10T 29/53657 (2015.01); Y10T 29/53683 (2015.01); Y10T 29/53843 (2015.01); Y10T 156/1105 (2015.01); Y10T 156/1906 (2015.01); Y10T 436/11 (2015.01); Y10T 436/111666 (2015.01); Y10T 436/113332 (2015.01); Y10T 436/114998 (2015.01); Y10T 436/119163 (2015.01); Y10T 436/2575 (2015.01);
Abstract

An automated analyzer for performing multiple diagnostic assays simultaneously includes multiple stations, or modules, in which discrete aspects of the assay are performed on fluid samples contained in reaction receptacles. The analyzer includes stations for automatically preparing a specimen sample, incubating the sample at prescribed temperatures for prescribed periods, performing an analyte isolation procedure, and ascertaining the presence of a target analyte. An automated receptacle transporting system moves the reaction receptacles from one station to the next. The analyzer further includes devices for carrying a plurality of specimen tubes and disposable pipette tips in a machine-accessible manner, a device for agitating containers of target capture reagents comprising suspensions of solid support material and for presenting the containers for machine access thereto, and a device for holding containers of reagents in a temperature controlled environment and presenting the containers for machine access thereto. A method for performing an automated diagnostic assay includes an automated process for isolating and amplifying a target analyte. The process is performed by automatically moving each of a plurality of reaction receptacles containing a solid support material and a fluid sample between stations for incubating the contents of the reaction receptacle and for separating the target analyte bound to the solid support from the fluid sample. An amplification reagent is added to the separated analyte after the analyte separation step and before a final incubation step.


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