Literature DB >> 8450232

Determination of antibody affinity by ELISA with a non-linear regression program. Evaluation of linearized approximations.

R W Glaser1.   

Abstract

ELISA experiments based on competition between immobilized and soluble antibody for soluble antigen, and on the formation of a ternary complex of immobilized antibody, antigen and soluble antibody were used by Hoylaerts et al. (J. Immunol. Methods 126 (1990) 253-261) for the determination of dissociation constants. The dissociation constant was taken from linearized plots according to a theory that required several approximations. The effect of these approximations on the resulting dissociation constants has been investigated using two computer programs, CBEIA-C and CBEIA-S. Since most approximations that have to be made for linearization can be avoided by non-linear regression, the programs provide a more reliable basis for calculation of the dissociation constant. Experiments measuring formation of a ternary complex were found to be unsuitable for affinity determination.

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Year:  1993        PMID: 8450232     DOI: 10.1016/0022-1759(93)90016-z

Source DB:  PubMed          Journal:  J Immunol Methods        ISSN: 0022-1759            Impact factor:   2.303


  2 in total

1.  The result of equilibrium-constant calculations strongly depends on the evaluation method used and on the type of experimental errors.

Authors:  H Fuchs; R Gessner
Journal:  Biochem J       Date:  2001-10-15       Impact factor: 3.857

2.  Mapping protein-protein contact sites using cellulose-bound peptide scans.

Authors:  U Reineke; R Sabat; A Kramer; R D Stigler; M Seifert; T Michel; H D Volk; J Schneider-Mergener
Journal:  Mol Divers       Date:  1996-05       Impact factor: 2.943

  2 in total

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