Abstract:
:The large scale production of a monoclonal anti-progesterone antibody in serum free medium followed by affinity chromatography on protein G lead to a contamination of the antibody sample with a protein of about 14 kDa. This protein was identified by mass spectrometry as secretory leukocyte protease inhibitor (SLPI). This SLPI contamination lead to a failure of the fiber-optic based competitive fluorescence assay to detect progesterone in milk. Purification of the monoclonal antibody using protein A columns circumvented this problem.
journal_name
J Biotechnoljournal_title
Journal of biotechnologyauthors
Schenk JA,Fettke J,Lenz C,Albers K,Mallwitz F,Gajovic-Eichelmann N,Ehrentreich-Förster E,Kusch E,Sellrie Fdoi
10.1016/j.jbiotec.2011.12.025subject
Has Abstractpub_date
2012-03-31 00:00:00pages
34-5issue
1-2eissn
0168-1656issn
1873-4863pii
S0168-1656(12)00002-8journal_volume
158pub_type
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