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Ryan T Duggan, 42Crestwood, IL

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Midlothian, IL   

Saint Charles, MO   

Wickliffe, KY   

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Maintenance Specialist

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Self Implo Ed
Maintenance Specialist
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Ryan Duggan

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Cambria Hotel Fort Mill

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Us Patents

Oligonucleotide-Mediated Quantitative Multiplexed Immunoassays

US Patent:
2017026, Sep 21, 2017
Filed:
May 26, 2017
Appl. No.:
15/606045
Inventors:
- Chicago IL, US
Ryan Duggan - Chicago IL, US
Stephen Kron - Chicago IL, US
International Classification:
C12Q 1/68
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.

Oligonucleotide-Mediated Quantitative Multiplexed Immunoassays

US Patent:
2015034, Dec 3, 2015
Filed:
Jun 14, 2013
Appl. No.:
14/408065
Inventors:
- Chicago IL, US
Ryan Duggan - Chicago IL, US
Stephen Kron - Chicago IL, US
International Classification:
C12Q 1/68
G01N 21/64
G01N 33/569
G01N 33/543
G01N 15/14
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.

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