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.
Patent No.:
Date of Patent:
Nov. 20, 2018
Filed:
Nov. 07, 2017
Applicant:
Fluidigm Corporation, South San Francisco, CA (US);
Inventors:
Marc Unger, San Mateo, CA (US);
Ian D. Manger, New York, NY (US);
Michael Lucero, South San Francisco, CA (US);
Yong Yi, San Francisco, CA (US);
Emily Miyashita-Lin, San Francisco, CA (US);
Anja Wienecke, Hamburg, DE;
Geoffrey Facer, San Francisco, CA (US);
Assignee:
Fluidigm Corporation, South San Francisco, CA (US);
Attorney:
Primary Examiner:
Int. Cl.
CPC ...
C12Q 1/68 (2018.01); C12P 19/34 (2006.01); B01L 3/00 (2006.01); C12Q 1/686 (2018.01); G01N 27/453 (2006.01); B01L 3/02 (2006.01); B01L 7/00 (2006.01);
U.S. Cl.
CPC ...
C12Q 1/68 (2013.01); B01L 3/5025 (2013.01); B01L 3/5027 (2013.01); B01L 3/50273 (2013.01); B01L 3/502707 (2013.01); B01L 3/502715 (2013.01); B01L 3/502738 (2013.01); C12Q 1/686 (2013.01); G01N 27/453 (2013.01); B01L 3/0248 (2013.01); B01L 7/52 (2013.01); B01L 2200/0642 (2013.01); B01L 2200/10 (2013.01); B01L 2200/142 (2013.01); B01L 2200/147 (2013.01); B01L 2300/06 (2013.01); B01L 2300/0636 (2013.01); B01L 2300/0816 (2013.01); B01L 2300/0819 (2013.01); B01L 2300/0861 (2013.01); B01L 2300/0864 (2013.01); B01L 2300/0867 (2013.01); B01L 2300/0874 (2013.01); B01L 2300/123 (2013.01); B01L 2300/1805 (2013.01); B01L 2400/0481 (2013.01); B01L 2400/0487 (2013.01); B01L 2400/06 (2013.01); B01L 2400/0638 (2013.01); B01L 2400/0655 (2013.01);
Abstract
A method for carrying out nucleic acid amplification reactions using a microfluidic device is described. Amplification primers and other amplification reagents are deposited at a plurality of reaction sites in the device, a sample solution containing amplifiable polynucleotides is introduced into the reaction sites, and amplification is carried out.