Platelet immunoglobulin bead suspension and flow cytometry

Chemistry: molecular biology and microbiology – Measuring or testing process involving enzymes or...

Reexamination Certificate

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C435S006120, C435S007100, C435S007200, C435S007930, C435S007940, C435S007950, C435S040510, C435S173400, C435S967000, C435S973000, C436S010000, C436S063000, C436S501000, C436S506000, C436S507000, C436S509000, C436S513000, C436S518000, C436S519000, C436S523000, C436S524000, C436S527000, C436S528000, C436S531000, C436S533000, C436S534000, C436S536000, C436S538000, C436S546000, C436S805000, C436S811000

Reexamination Certificate

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06933106

ABSTRACT:
Immunoassay methods and apparatus are provided which utilize flow cytometry, coated latex microspheres, and fluorochrome labeled antibodies, to simultaneously detect the presence and amount of one or more analytes in a sample. By combining FALS and fluorescence, it is practical to use beads of several different sizes, colors or shapes, each bead coated with a different analyte, for the simultaneous detection of one or more analytes and of cell components such as platelets in a sample.

REFERENCES:
patent: 6268222 (2001-07-01), Chandler et al.
patent: 6280618 (2001-08-01), Watkins et al.
patent: 2003/0008410 (2003-01-01), Hechinger
patent: 2003/0032068 (2003-02-01), Hechinger
Greenwalt et al. An enzyme linked antiglobulin test to quantify nanogram quantities of IgG on polystyrene microspheres. Vox Sang. 63 (4) pp. 272-275 (1992).
Rosenfeld et al., Detection of platelet alloantibodies by flow cytometry. Characterization and Clinical Significance. Am J Clin. Path. 85(2), pp. 207-212 (1986).

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