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:
May. 30, 2017

Filed:

Jun. 14, 2013
Applicant:

The University of Chicago, Chicago, IL (US);

Inventors:

Amy Flor, Chicago, IL (US);

Ryan Duggan, Chicago, IL (US);

Stephen Kron, Chicago, IL (US);

Assignee:

The University of Chicago, Chicago, IL (US);

Attorney:
Primary Examiner:
Int. Cl.
CPC ...
G01N 15/14 (2006.01); C12Q 1/68 (2006.01); G01N 33/543 (2006.01); G01N 33/569 (2006.01); G01N 21/64 (2006.01); G01N 33/68 (2006.01); G01N 15/10 (2006.01); G01N 15/00 (2006.01);
U.S. Cl.
CPC ...
C12Q 1/6804 (2013.01); C12Q 1/6811 (2013.01); G01N 15/14 (2013.01); G01N 21/6486 (2013.01); G01N 33/54326 (2013.01); G01N 33/54333 (2013.01); G01N 33/56966 (2013.01); G01N 33/56972 (2013.01); G01N 33/6854 (2013.01); G01N 2015/008 (2013.01); G01N 2015/0065 (2013.01); G01N 2015/1006 (2013.01); G01N 2015/1402 (2013.01); G01N 2458/10 (2013.01);
Abstract

Methods and compositions for quantitative immunoassays are provided, in which ligand-conjugated probes are used to label samples and ligand-surfaced microspheres are used as quantitative reference standards. Certain embodiments provide a method of quantitative flow cytometry where ligands are oligonucleotides, and a sample comprising one or more cells is contacted with a hybridized antibody::fluorophore labeled targeting construct to label the cells, and the labeled cells are analyzed. In some embodiments, a population of quantitative labeled oligospheres labeled with the same fluorescent label as the cells is analyzed using the flow cytometer and used to create a quantitative standard curve of cytometer intensity versus molecules fluorescent label per oligosphere event. A standard curve trendline is established and used to determine the molecules of fluorescent label per cellular event for the antigen-positive cell populations. Based on molecules of fluorescent label per cell, the amount of Antibody Binding per Cell (ABC) is quantified.


Find Patent Forward Citations

Loading…