skip to main content
DOE Patents title logo U.S. Department of Energy
Office of Scientific and Technical Information

Title: Method of identity analyte-binding peptides

Abstract

A method for affinity chromatography or adsorption of a designated analyte utilizes a paralog as the affinity partner. The immobilized paralog can be used in purification or analysis of the analyte; the paralog can also be used as a substitute for antibody in an immunoassay. The paralog is identified by screening candidate peptide sequences of 4--20 amino acids for specific affinity to the analyte. 5 figs.

Inventors:
Issue Date:
Research Org.:
Terrapin Diagnostics Ltd
OSTI Identifier:
7267631
Patent Number(s):
4963263 A
Application Number:
PPN: US 7-355042
Assignee:
Terrapin Technologies, Inc., San Francisco, CA (United States)
DOE Contract Number:  
AC03-88ER80678
Resource Type:
Patent
Resource Relation:
Patent File Date: 16 May 1989
Country of Publication:
United States
Language:
English
Subject:
37 INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY; 59 BASIC BIOLOGICAL SCIENCES; MATERIALS; ADSORPTION; PEPTIDES; AMINO ACID SEQUENCE; MATERIALS RECOVERY; MEASURING METHODS; TECHNOLOGY ASSESSMENT; MANAGEMENT; MOLECULAR STRUCTURE; ORGANIC COMPOUNDS; PROCESSING; PROTEINS; SORPTION; WASTE MANAGEMENT; WASTE PROCESSING; 400105* - Separation Procedures; 550200 - Biochemistry

Citation Formats

Kauvar, L M. Method of identity analyte-binding peptides. United States: N. p., 1990. Web.
Kauvar, L M. Method of identity analyte-binding peptides. United States.
Kauvar, L M. Tue . "Method of identity analyte-binding peptides". United States.
@article{osti_7267631,
title = {Method of identity analyte-binding peptides},
author = {Kauvar, L M},
abstractNote = {A method for affinity chromatography or adsorption of a designated analyte utilizes a paralog as the affinity partner. The immobilized paralog can be used in purification or analysis of the analyte; the paralog can also be used as a substitute for antibody in an immunoassay. The paralog is identified by screening candidate peptide sequences of 4--20 amino acids for specific affinity to the analyte. 5 figs.},
doi = {},
journal = {},
number = ,
volume = ,
place = {United States},
year = {1990},
month = {10}
}