U.S. patents available from 1976 to present.
U.S. patent applications available from 2005 to present.

Method for carrying out non-isotopic immunoassays, labeled analytes and kits for use in such assays

Patent 4378428 Issued on March 29, 1983. Estimated Expiration Date: Icon_subject March 30, 2001. Estimated Expiration Date is calculated based on simple USPTO term provisions. It does not account for terminal disclaimers, term adjustments, failure to pay maintenance fees, or other factors which might affect the term of a patent.

Patent References

3817837

3843696

3852157

3856469

3875011

3884898

3888866

3905871

3917582

Antibody steric hindrance immunoassay with two antibodies
Patent #: 3935074
Issued on: 01/27/1976
Inventor: Rubenstein ,   et al.

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Inventors

Assignee

Application

No. 06/248689 filed on 03/30/1981

US Classes:

435/7.23, Tumor cell or cancer cell435/188, Stablizing an enzyme by forming a mixture, an adduct or a composition, or formation of an adduct or enzyme conjugate435/7.4, To identify an enzyme or isoenzyme435/7.7, Assay in which a label present is an apoenzyme, prosthetic group, or enzyme cofactor435/7.8, Involving nonmembrane bound receptor binding or protein binding other than antigen-antibody binding435/7.93, Competitive assay435/810, PACKAGED DEVICE OR KIT435/967, STANDARDS, CONTROLS, MATERIALS (E.G., VALIDATION STUDIES, BUFFER SYSTEMS, ETC.)435/968, HIGH ENERGY SUBSTRATES (E.G., FLUORESCENT, CHEMILUMINESCENT, RADIOACTIVE, ETC.)435/971, CAPTURE OF COMPLEX AFTER ANTIGEN-ANTIBODY REACTION435/975, KIT436/500, THYROID HORMONE TESTS (E.G., T3, T4, TBG, TSH, ETC.)436/518, INVOLVING AN INSOLUBLE CARRIER FOR IMMOBILIZING IMMUNOCHEMICALS436/528, Carrier is organic436/532, Antigen or antibody attached to a carrier via bridging agent436/536, INVOLVING IMMUNE COMPLEX FORMED IN LIQUID PHASE436/544, Producing labeled antigens530/345, Chemical aftertreatment, e.g., acylation, methylation, etc.530/389.2, Binds hormone, lymphokine, cytokine, or other secreted growth regulatory factor, differentiation factor, intercellular mediator, or neurotransmitter (e.g., insulin, human chorionic gonadotropin, glucagon, cardiodilatin, interleukin, interferon, norepinephrine, epinephrine, acetylcholine, etc.)530/389.3, Binds plasma protein, serum protein, or fibrin (e.g., clotting factor, fibrinolytic factor, complement factor, immunoglobulin, apolipoprotein, etc.)530/389.7, Binds cancer cell or component or product thereof (e.g., cell-surface antigen, etc.)530/389.8, Binds drug, hapten, hapten-carrier complex, or specifically-identified chemical structure (e.g., theophylline, digoxin, etc.)530/404, Sulfur containing reactant530/408, Sulfur containing reactant930/10, PEPTIDE OR PROTEIN SEQUENCE930/240Enzyme or isoenzyme

Examiners

Primary: Wiseman, Thomas G.

Attorney, Agent or Firm

International Classes

G01N 33/58 (20060101)
G01N 33/535 (20060101)
G01N 33/542 (20060101)
G01N 33/536 (20060101)

Abstract

A highly sensitive, immunoassay method for determining the amount of an analyte in a sample containing a known analyte in an unknown concentration is provided. Sample; a polypeptide-labeled analog of the analyte, an antibody specific for said analyte, a polypeptide partner capable of non-covalently binding with the polypeptide-labeled analyte to form a complex having catalytic activity, and a substrate capable of being converted to a reporter molecule by the catalytic activity of said complex are brought together in a medium. The polypeptide-labeled analyte analog is capable of competitively binding to the antibody and the polypeptide partner, the antibody inhibiting the formation of a catalytically active complex in the absence of analyte, and the concentrations of the antibody, polypeptide partner and polypeptide-labeled analyte are such as to cause varying amounts of analyte to be directly related to the conversion of the substrate to the reporter molecule. Conversion of the substrate to the reporter molecule is then determined, and compared to conversions of substrate to reporter molecule obtained with known concentrations of the analyte.

Other References

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