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. 24, 2020

Filed:

Aug. 22, 2018
Applicant:

California Institute of Technology, Pasadena, CA (US);

Inventors:

Aditya Rajagopal, Orange, CA (US);

Mark D. Goldberg, Alta Loma, CA (US);

Erika F. Garcia, Los Angeles, CA (US);

Xiomara L. Madero, Glendale, CA (US);

Thomas A. Tombrello, Altadena, CA (US);

Axel Scherer, Barnard, VT (US);

Assignee:
Attorney:
Primary Examiner:
Int. Cl.
CPC ...
C12P 19/34 (2006.01); C12Q 1/70 (2006.01); C12Q 1/68 (2018.01); C12Q 1/6851 (2018.01);
U.S. Cl.
CPC ...
C12Q 1/701 (2013.01); C12Q 1/68 (2013.01); C12Q 1/6851 (2013.01); C12Q 1/703 (2013.01); Y10T 436/143333 (2015.01);
Abstract

Methods and kits for detecting a genetic variation in a polynucleotide analyte in a sample. A fluorophore is attached to a first primer, a quencher is attached to a second primer, and the first primer and the second primer are specific for the polynucleotide analyte. At least one of the primers is configured to hybridize to a region of the polynucleotide analyte encoding the genetic variation. The primers are configured to amplify the polynucleotide analyte having the genetic variation and a corresponding polynucleotide analyte lacking the generic variation. There is a detectable difference between a change in signal generated by the fluorophore and quencher when using the first and second primers to amplify the polynucleotide analyte with the genetic variation, and a change in signal generated by the fluorophore and quencher when using the first and second primers to amplify the corresponding polynucleotide analyte lacking the genetic variation.


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