A sensitive enzyme immunoassay for human basic fibroblast growth factor

https://doi.org/10.1016/S0006-291X(05)81224-0Get rights and content

Summary

A sensitive sandwich enzyme immunoassay for human basic fibroblast growth factor (HbFGF) was developed employing three monoclonal antibodies (MAb3H3, MAb98 and MAb52). The Fab' fragment of MAb3H3 which inhibits HbFGF biological activity was conjugated to horseradish peroxidase. A mixture of MAb52 and MAb98 was used in the solid phase. Neiter human acidic fibroblast growth factor, hst-1/KS3 product nor acid denatured HbFGF was cross-reactive in this assay system. The detection limit of this assay system was 1 pg/well. Using this assay, some tumor cell lines were revealed to produce a higher level of bFGF than a normal one. Serum samples from normal volunteers were also assayed, and immuno-reactive HbFGF could be detected in 16 out of 57 samples at range 30∼206 pg/ml.

References (19)

  • GospodarowiczD.

    Methods in Enzymol.

    (1987)
  • IwaneM. et al.

    Biochem. Biophys. Res. Commun.

    (1987)
  • PavluB. et al.

    J. Chromato.

    (1986)
  • KurokawaT. et al.

    FEBS Lett.

    (1987)
  • SakaguchiM. et al.

    FEBS Lett.

    (1988)
  • LobbR. et al.

    J. Biol. Chem

    (1986)
  • BurgessW.H. et al.

    Annu. Rev. Biochem.

    (1989)
  • SenoM. et al.

    Hybridoma

    (1989)
  • SatoY. et al.

    Mol. Endcrinol.

    (1989)
There are more references available in the full text version of this article.

Cited by (76)

  • Engineering strategies to recapitulate the tumor microenvironment

    2015, Cells, Forces, and the Microenvironment
View all citing articles on Scopus
View full text