Literature DB >> 24234098

Biospecific reversible immobilization : A method for introducing labile structures into analytical systems.

B Mattiasson1.   

Abstract

Immobilized lectins placed in continuous flow systems were used for biospecific reversible immobilization of labile biochemical structures, e.g., enzymes such as ascorbic acid oxidase and acetylcholine esterase, and cells, such as red blood cells and lymphocytes. The species thus immobilized were applied in continuous flow analytical processes.

Year:  1982        PMID: 24234098     DOI: 10.1007/BF02798633

Source DB:  PubMed          Journal:  Appl Biochem Biotechnol        ISSN: 0273-2289            Impact factor:   2.926


  4 in total

1.  Assay procedures for immobilized enzymes.

Authors:  B Mattiasson; K Mosbach
Journal:  Methods Enzymol       Date:  1976       Impact factor: 1.600

2.  Isolation of leucocytes from human blood. Further observations. Methylcellulose, dextran, and ficoll as erythrocyteaggregating agents.

Authors:  A Böyum
Journal:  Scand J Clin Lab Invest Suppl       Date:  1968

3.  A general enzyme thermistor based on specific reversible immobilization using the antigen--antibody interaction. Assay of hydrogen peroxide, penicillin, sucrose, glucose, phenol and tyrosine.

Authors:  B Mattiasson
Journal:  FEBS Lett       Date:  1977-05-01       Impact factor: 4.124

4.  An analytical flow system based on reversible immobilization of enzymes and whole cells utilizing specific lectin-glucoprotein interactions.

Authors:  B Mattiasson; C Borrebaeck
Journal:  FEBS Lett       Date:  1978-01-01       Impact factor: 4.124

  4 in total

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