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:
Oct. 08, 2019

Filed:

Nov. 06, 2017
Applicant:

Micronics, Inc., Redmond, WA (US);

Inventors:

C. Frederick Battrell, Wenatchee, WA (US);

Troy D. Daiber, Auburn, WA (US);

William Samuel Hunter, Jan Juc, AU;

Assignee:

MICRONICS, INC., Redmond, WA (US);

Attorney:
Primary Examiner:
Int. Cl.
CPC ...
G01N 21/64 (2006.01); B01L 3/00 (2006.01); B01L 7/00 (2006.01);
U.S. Cl.
CPC ...
G01N 21/6428 (2013.01); B01L 3/502715 (2013.01); B01L 7/52 (2013.01); G01N 21/645 (2013.01); B01L 2200/0684 (2013.01); B01L 2300/0816 (2013.01); B01L 2300/168 (2013.01); B01L 2300/1827 (2013.01); B01L 2300/1844 (2013.01); B01L 2400/0487 (2013.01); G01N 2201/062 (2013.01); G01N 2201/12 (2013.01); Y02A 90/26 (2018.01);
Abstract

A compact, microprocessor-controlled instrument for fluorometric assays in liquid samples has a floating stage with docking bay for receiving a microfluidic cartridge and a scanning detector head with on-board embedded microprocessor controlled by an optical data acquisition and processing daemon within the detector head for controlling source LEDs, emission signal amplification and filtering in an isolated, low noise, high-gain environment within the detector head. Multiple optical channels may be incorporated in the scanning head. The assay ma be validated using dual channel optics for monitoring a first fluorophore associated with a target analyte and a second fluorophore associated with a control. Molecular biological assays use PCR amplification of target nucleic acids and fluorometric assays, which may require temperature control during detection. Sensitivity and resistance to bubble interference during scanning are improved using a heating block with reflective mirror face in contact with a thermo-optical window enclosing the liquid sample.


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