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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.

Patent No.:

US 11708595 B1

PDFFull Text
Date of Patent:
Jul. 25, 2023

Filed:

Jan. 14, 2020

Nanostructured biomimetic protein superconductive devices of making and its multiple applications thereto

Applicant:

Ellen Tuanying Chen, Rockville, MD (US);

Inventor:

Ellen Tuanying Chen, Rockville, MD (US);

Assignee:

Other;

Attorney:
Primary Examiner:

Quan Tra

Int. Cl.
CPC ...
G06N 10/40 (2022.01); C12Q 1/00 (2006.01); G01N 27/414 (2006.01); G01N 33/543 (2006.01); G01N 27/327 (2006.01); H10N 60/12 (2023.01); H10N 60/00 (2023.01); H10N 60/80 (2023.01); H10N 60/85 (2023.01); H10N 69/00 (2023.01); B82Y 5/00 (2011.01);
U.S. Cl.
CPC ...
C12Q 1/002 (2013.01); G01N 27/3278 (2013.01); G01N 27/4145 (2013.01); G01N 27/4146 (2013.01); G01N 33/5438 (2013.01); H10N 60/12 (2023.02); H10N 60/805 (2023.02); H10N 60/851 (2023.02); H10N 60/99 (2023.02); H10N 69/00 (2023.02); B82Y 5/00 (2013.01);
Abstract

A multiple functioning superconductive device was invented based on Toroidal Josephson Junction (FFTJJ) array with 3D-cage structure self-assembled organo-metallic superlattice membrane. The device not only mimics the structure and function of an activated Matrix Metalloproteinase-2 (MMP-2) protein, but also mimics the cylinder structure of the Heat Shock Protein (HSP60) protein, that works at room temperature under a normal atmosphere, and without external electromagnetic power applied. The device enabled direct rapid real-time monitoring atto-molarity concentration ATP in biological specimens and was able to define the anti-inflammatory and pro-inflammatory status revealed a transitional range of ATP concentration under antibody-free, tracer-free and label-free conditions.

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