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. 28, 2023

Filed:

Dec. 02, 2020
Applicant:

Bio-rad Laboratories, Inc., Hercules, CA (US);

Inventors:

Kevin D. Ness, Pleasanton, CA (US);

Donald A. Masquelier, Tracy, CA (US);

Billy W. Colston, Jr., San Ramon, CA (US);

Benjamin J. Hindson, Livermore, CA (US);

Assignee:

Bio-Rad Laboratories, Inc., Hercules, CA (US);

Attorney:
Primary Examiner:
Int. Cl.
CPC ...
B01L 3/00 (2006.01); B01L 3/02 (2006.01); B01L 7/00 (2006.01); G01N 21/3563 (2014.01); B01F 23/41 (2022.01); B01F 33/3011 (2022.01); B01F 35/10 (2022.01); C12Q 1/686 (2018.01); G01N 21/64 (2006.01); B29C 45/00 (2006.01); G01N 21/49 (2006.01); B01F 101/23 (2022.01); B29L 31/00 (2006.01);
U.S. Cl.
CPC ...
B01L 3/502784 (2013.01); B01F 23/41 (2022.01); B01F 33/3011 (2022.01); B01F 35/10 (2022.01); B01L 3/0241 (2013.01); B01L 3/502715 (2013.01); B01L 7/525 (2013.01); B29C 45/006 (2013.01); B29C 45/0053 (2013.01); C12Q 1/686 (2013.01); G01N 21/3563 (2013.01); G01N 21/49 (2013.01); G01N 21/6428 (2013.01); G01N 21/6486 (2013.01); B01F 23/4143 (2022.01); B01F 23/4145 (2022.01); B01F 2101/23 (2022.01); B01L 7/52 (2013.01); B01L 2200/0673 (2013.01); B01L 2200/0689 (2013.01); B01L 2200/10 (2013.01); B01L 2200/12 (2013.01); B01L 2300/041 (2013.01); B01L 2300/0654 (2013.01); B01L 2300/0816 (2013.01); B01L 2300/0819 (2013.01); B01L 2300/0858 (2013.01); B01L 2300/0867 (2013.01); B01L 2300/1822 (2013.01); B01L 2400/049 (2013.01); B01L 2400/0478 (2013.01); B01L 2400/0487 (2013.01); B01L 2400/0622 (2013.01); B29C 2045/0079 (2013.01); B29L 2031/752 (2013.01); G01N 2021/6439 (2013.01); Y02A 90/10 (2018.01);
Abstract

Method of analysis. In the method, a first emulsion and a second emulsion substantially separated from one another by a spacer fluid may be formed. The first emulsion, the spacer fluid, and the second emulsion may be flowed in a channel from a fluid inlet to a fluid outlet of a heating and cooling station having two or more temperature-controlled zones, such that each emulsion is thermally cycled to promote amplification of a nucleic acid target in droplets of the emulsion. Amplification data may be collected from individual droplets of each emulsion downstream of the heating and cooling station. A level of the nucleic acid target present in each emulsion may be determined based on the amplification data collected from the individual droplets of the emulsion.


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