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PMID: 1629607 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Production and characterisation of monoclonal antibodies against native and disassembled human catalase.

Journal of immunological methods ·Vol. 151 ·No. 1-2 ·1992-07-06 ·Pages 165-75

Wiemer EA, Ofman R, Middelkoop E, de Boer M, Wanders RJ, Tager JM

Abstract

Catalase isolated from human erythrocytes was used to immunise mice, in order to generate hybridomas producing specific monoclonal antibodies to the enzyme. Hybridomas secreting anti-(catalase) antibodies were identified by a modified enzyme-linked immunosorbent assay (ELISA) using either monomer/dimer catalase or native, tetrameric enzyme. Three stable hybridoma clones were selected and the characteristics of the antibodies produced were investigated by ELISA, immunofluorescence, immunoprecipitation and immunoblotting experiments. One monoclonal antibody (17E10) was shown to interact with both native tetramer catalase and--to a lesser extent--with monomer/dimer catalase. Two monoclonal antibodies (10B12H9, 13A10) were found to react only with completely denatured catalase or with monomer/dimer catalase but not with native catalase.

MeSH Terms
Antibodies, Monoclonal/immunology Catalase/chemistry,immunology Humans Hybridomas/immunology Macromolecular Substances Molecular Structure Protein Conformation Structure-Activity Relationship
Chemicals
Antibodies, Monoclonal Macromolecular Substances Catalase
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Wiemer E A
E.C. Slater Institute for Biochemical Research, University of Amsterdam, Netherlands.
Ofman R
Middelkoop E
de Boer M
Wanders R J
Tager J M
Article Info
Journal
Journal of immunological methods
Abbr.
J Immunol Methods
ISSN
0022-1759
Published
1992-07-06
Pages
165-75
Language
English
Region
Netherlands
NLM ID
1305440
Subset
IM
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