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:
Jun. 16, 2020

Filed:

May. 27, 2014
Applicant:

Nova Southeastern University, Fort Lauderdale, FL (US);

Inventors:

Stephen G. Grant, Fort Lauderdale, FL (US);

Jean J. Latimer, Fort Lauderdale, FL (US);

Assignee:

NOVA SOUTHEASTERN UNIVERSITY, Fort Lauderdale, FL (US);

Attorneys:
Primary Examiner:
Int. Cl.
CPC ...
G01N 33/80 (2006.01); G01N 33/50 (2006.01);
U.S. Cl.
CPC ...
G01N 33/80 (2013.01); G01N 33/5005 (2013.01); G01N 33/5091 (2013.01); G01N 33/5094 (2013.01); G01N 2333/70596 (2013.01); G01N 2800/28 (2013.01);
Abstract

In the detection of a complex multifactorial disease, an MN blood group typing is performed on a first blood sample of a subject to be tested for a complex multifactorial disease, and on a second blood sample of a control subject having known phenotypes. Erythrocytes from the samples are isovolumetrically sphered, and M alleles and N alleles expressed on surfaces of erythrocyte cells of the first and second blood samples are labeled by contacting the blood samples with anti-M antibodies and anti-N antibodies associated with a marker. Labeled M alleles and labeled N alleles in the first and second blood samples are detected and quantified using the marker, in order to determine an incidence of somatic mutations in Glycophorin A of the patient. The incidence is compared with data pertaining to patients with a known complex multifactorial disease, to diagnose the patient.


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