NDLI: Development of a Luminescence Immunoassay for Follitropin Suitable for Clinical Routine

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Development of a Luminescence Immunoassay for Follitropin Suitable for Clinical Routine

Content Provider	Scilit
Author	Biro, G. Samira, Asfoura Butz, H. Leicht, E. Weinges, K. F.
Copyright Year	1991
Abstract	We developed a luminescence immunoassay (LIA) for follitropin, based on the synthesis of a follitropin-N-(4-aminobutyl)-N-ethylisoluminol conjugate. The luminescence tracer was purified by gel chromatography. Antibody-bound and non-bound tracer fractions were separated by using a second antibody reagent bound to magnetic particles. The assay can be performed within 24 hours and is sufficiently sensitive for the measurement of all clinically relevant follitropin concentrations including the subnormal range.
Related Links	https://edoc.hu-berlin.de/bitstream/18452/12437/1/cclm.1991.29.3.189.pdf http://www.degruyter.com/downloadpdf/j/cclm.1991.29.issue-3/cclm.1991.29.3.189/cclm.1991.29.3.189.xml
Ending Page	192
Page Count	4
Starting Page	189
ISSN	14346621
e-ISSN	14374331
DOI	10.1515/cclm.1991.29.3.189
Journal	Clinical Chemistry and Laboratory Medicine (CCLM)
Issue Number	3
Volume Number	29
Language	English
Publisher	Walter de Gruyter GmbH
Publisher Date	1991-01-01
Access Restriction	Open
Subject Keyword	Clinical Chemistry and Laboratory Medicine (cclm) Analytical Chemistry Antibody Chromatography Tracer Routine Sufficiently Follitropin Ethylisoluminol Luminescence Immunoassay Journal: Clinical Chemistry and Laboratory Medicine (CCLM), Vol- 29
Content Type	Text
Resource Type	Article
Subject	Biochemistry (medical) Clinical Biochemistry

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