Literature DB >> 7452000

A general and mild procedure for the purification of rabbit Fab' antibodies.

E Ishikawa, S Yoshitake.   

Abstract

A mild procedure for the purification of rabbit Fab' antibodies is described. A small column of normal goat IgG-Sepharose 4B (3 cm x 5mm) was saturated with F(ab')2 prepared from rabbit anti-goat IgG, and anti-goat IgG Fab was eluted from the column by splitting the disulfide bond in the hinge of the F(ab')2 molecule using 10 or 12 mM 2-mercaptoethylamine at pH 7. The recovery of anti-goat IgG Fab' in the eluate was about 35% of anti-goat IgG F(ab')2 bound to the column, and the purity of anti-goat IgG Fab' eluted was more than 90%. This procedure may be applicable to most kinds of rabbit IgG antibodies and useful for various immunoassays.

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Year:  1980        PMID: 7452000     DOI: 10.1016/0022-1759(80)90336-1

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


  1 in total

1.  GingisKHAN™ protease cleavage allows a high-throughput antibody to Fab conversion enabling direct functional assessment during lead identification of human monoclonal and bispecific IgG1 antibodies.

Authors:  Jörg Moelleken; Manuel Endesfelder; Christian Gassner; Sabine Lingke; Simone Tomaschek; Oksana Tyshchuk; Stefan Lorenz; Ulrike Reiff; Michael Mølhøj
Journal:  MAbs       Date:  2017-08-14       Impact factor: 5.857

  1 in total

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