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. 23, 2021

Filed:

Jul. 15, 2019
Applicant:

Vala Sciences, Inc., San Diego, CA (US);

Inventors:

Fabio Cerignoli, San Diego, CA (US);

Piyush Gehalot, San Diego, CA (US);

Patrick M. McDonough, San Diego, CA (US);

Jeffrey H. Price, San Diego, CA (US);

Ross J. Whittaker, San Diego, CA (US);

Assignee:

Vala Sciences, Inc., San Diego, CA (US);

Attorney:
Primary Examiner:
Int. Cl.
CPC ...
G01N 21/27 (2006.01); G02B 21/36 (2006.01); H04N 5/247 (2006.01); H04N 5/232 (2006.01); H04N 5/91 (2006.01); G01J 3/28 (2006.01); G01J 3/44 (2006.01); G01N 21/64 (2006.01); G01N 33/52 (2006.01);
U.S. Cl.
CPC ...
G01N 21/272 (2013.01); G01J 3/2823 (2013.01); G01J 3/4406 (2013.01); G01N 21/6408 (2013.01); G01N 21/6428 (2013.01); G01N 21/6458 (2013.01); G01N 33/52 (2013.01); G02B 21/365 (2013.01); H04N 5/23212 (2013.01); H04N 5/232133 (2018.08); H04N 5/247 (2013.01); H04N 5/91 (2013.01); G01N 2021/6421 (2013.01); G01N 2021/6441 (2013.01);
Abstract

Video recordings from two or more optical channels are produced, processed, and analyzed simultaneously in order to provide quantitative analysis of action potentials, calcium transients and ionic flux in excitable cells loaded with voltage or ion sensitive dyes with distinct excitation and emission wavelengths. The specific wavelengths of fluorescent light emitted from each dye are separated and recorded. The recordings are mutually registered and cytometric analysis is performed to provide a quantitative analysis of the action potentials, calcium transient, and/or ionic flux on a cell-by-cell and well-by-well basis in microtiter plates. The cells are then fixed, labeled for other biomarkers, and scanned again. The resulting fixed cell images are registered with the live cell recordings and analyzed; missing cells that were washed off are detected relative to the live recordings, and cytometry data from live and fixed cell scans is collated cell-by-cell.


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