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:
Jan. 11, 1983

Filed:

Apr. 27, 1981
Applicant:
Inventors:

Joseph D Andrade, Salt Lake City, UT (US);

Richard Van Wagenen, Salt Lake City, UT (US);

Assignee:

University of Utah Research Foundation, Salt Lake City, UT (US);

Attorney:
Primary Examiner:
Int. Cl.
CPC ...
G01N / ; G01N / ; G01N / ;
U.S. Cl.
CPC ...
435-4 ; 435-5 ; 435-7 ; 435 34 ; 436517 ; 436540 ; 436546 ; 436805 ; 436815 ; 436817 ; 436816 ;
Abstract

A process is presented for conducting fluorescence immunoassays without the use of added labels by utilizing ultraviolet radiation and internal reflection optics to activate fluorescent groups present in the molecules of interest. The assay is accomplished by directing a beam of light having wavelengths in the ultraviolet region to a solid liquid interface which (1) has a material X immobilized thereon, and (2) is contacted with an assay solution containing in unknown Y which contains intrinsic tyrosine, tryptophan, nucleic acid or related fluorescence groups which are activated by wavelengths in the ultraviolet region; X and Y may be in the relationship of antibody and antigen in that one had the ability of recognizing the particular spatial and polar configuration of the other and is attracted to and bound to such configuration, said beam of ultraviolet light being projected under such conditions that there is internal reflection at the interface, and then measuring the amount of fluorescence emitted from the surface of the interface, the amount of the fluorescence emission being a function of the amount of the unknown Y being detected. In the event that Y is not fluorescent, the X-Y sandwich can be further exposed to a solution containing X, to form XYX sandwich. The observed fluorescence of X is proportional to the amount of bound Y which is in turn related to the solution concentration of Y.


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