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:
Aug. 24, 2021

Filed:

Jul. 07, 2015
Applicants:

National Institute of Advanced Industrial Science and Technology, Tokyo, JP;

Kyorin Pharmaceutical Co., Ltd., Tokyo, JP;

Inventors:

Hidenori Nagai, Ikeda, JP;

Shunsuke Furutani, Ikeda, JP;

Yoshihisa Hagihara, Ikeda, JP;

Yusuke Fuchiwaki, Takamatsu, JP;

Attorney:
Primary Examiner:
Int. Cl.
CPC ...
C12Q 1/686 (2018.01); B01L 7/00 (2006.01); C12N 15/09 (2006.01); C12M 1/00 (2006.01); B01L 3/00 (2006.01); C12Q 1/6851 (2018.01);
U.S. Cl.
CPC ...
C12Q 1/686 (2013.01); B01L 3/502715 (2013.01); B01L 7/525 (2013.01); C12M 1/00 (2013.01); C12N 15/09 (2013.01); C12Q 1/6851 (2013.01); B01L 2300/0654 (2013.01); B01L 2300/0883 (2013.01); B01L 2400/0475 (2013.01); Y02A 40/70 (2018.01);
Abstract

The present invention provides a reciprocal-flow-type nucleic acid amplification device comprising: heaters capable of forming a denaturation temperature zone and an extension/annealing temperature zone; a fluorescence detector capable of detecting movement of a sample solution between the two temperature zones; a pair of liquid delivery mechanisms that allow the sample solution to move between the two temperature zones and that are configured to be open to atmospheric pressure when liquid delivery stops; a substrate on which the chip for nucleic acid amplification according to claimcan be placed; and a control mechanism that controls driving of each liquid delivery mechanism by receiving an electrical signal from the fluorescence detector relating to movement of the sample solution from the control mechanism; the device being capable of performing real-time PCR by measuring fluorescence intensity for each thermal cycle.


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