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:
Aug. 26, 2025

Filed:

Jul. 12, 2023
Applicants:

Mcbi Inc., Tsukuba, JP;

University of Tsukuba, Tsukuba, JP;

Inventors:

Kazuhiko Uchida, Tsukuba, JP;

Kohji Meno, Tsukuba, JP;

Hideaki Suzuki, Tsukuba, JP;

Yoshinori Nishimura, Tsukuba, JP;

Assignees:

MCBI INC., Tokyo, JP;

UNIVERSITY OF TSUKUBA, Tsukuba, JP;

Attorney:
Primary Examiner:
Assistant Examiner:
Int. Cl.
CPC ...
G01N 33/68 (2006.01); C07K 14/47 (2006.01);
U.S. Cl.
CPC ...
G01N 33/6893 (2013.01); C07K 14/47 (2013.01); G01N 2333/76 (2013.01); G01N 2333/775 (2013.01); G01N 2333/96433 (2013.01); G01N 2800/2814 (2013.01);
Abstract

Biomarkers for detecting cognitive dysfunction diseases and methods for detecting cognitive dysfunction diseases using the biomarkers are provided. A method for detecting cognitive dysfunction diseases comprising measuring one or more biomarkers for detecting cognitive dysfunction diseases selected from the following (a), (b), and (c) in a biological sample simultaneously or separately: (a) a biomarker for detecting cognitive dysfunction diseases consisting of an intact protein of apolipoprotein A1 comprising the amino acid sequence represented by SEQ ID NO:1 or a partial peptide thereof; (b) a biomarker for detecting cognitive dysfunction diseases consisting of an intact protein of transthyretin comprising the amino acid sequence represented by SEQ ID NO:2 or a partial peptide thereof; and (c) a biomarker for detecting cognitive dysfunction diseases consisting of an intact protein of complement C3 comprising the amino acid sequence represented by SEQ ID NO:3 or a partial peptide thereof.


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