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:
Feb. 01, 2022

Filed:

May. 25, 2018
Applicant:

Caliper Life Sciences, Inc., Hopkinton, MA (US);

Inventors:

Morten J. Jensen, San Francisco, CA (US);

Andrea W. Chow, Los Altos, CA (US);

Colin B. Kennedy, Greenbrae, CA (US);

Stephane Mouradian, Menlo Park, CA (US);

Assignee:

Caliper Life Sciences, Inc., Hopkinton, MA (US);

Attorneys:
Primary Examiner:
Int. Cl.
CPC ...
B01L 7/00 (2006.01); B01L 3/00 (2006.01);
U.S. Cl.
CPC ...
B01L 7/525 (2013.01); B01L 3/5027 (2013.01); B01L 3/502715 (2013.01); B01L 3/502746 (2013.01); B01L 7/5255 (2013.01); B01L 3/5025 (2013.01); B01L 3/50851 (2013.01); B01L 2300/0609 (2013.01); B01L 2300/087 (2013.01); B01L 2300/0816 (2013.01); B01L 2300/0829 (2013.01); B01L 2300/0864 (2013.01); B01L 2300/0867 (2013.01); B01L 2300/0877 (2013.01); B01L 2300/1822 (2013.01); B01L 2300/1827 (2013.01); B01L 2400/0418 (2013.01); B01L 2400/0487 (2013.01);
Abstract

Embodiments of the invention comprise microfluidic devices, instrumentation interfacing with those devices, processes for fabricating that device, and methods of employing that device to perform PCR amplification. Embodiments of the invention are also compatible with quantitative Polymerase Chain Reaction ('qPCR') processes. Microfluidic devices in accordance with the invention may contain a plurality of parallel processing channels. Fully independent reactions can take place in each of the plurality of parallel processing channels. The availability of independent processing channels allows a microfluidic device in accordance with the invention to be used in a number of ways. For example, separate samples could be processed in each of the independent processing channels. Alternatively, different loci on a single sample could be processed in multiple processing channels.


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