Abstract
Summary Gangliosides inhibit the binding of 125 I-labeled luteinizing hormone to rat testis membranes. The inhibition is the result of an interaction between the hormone and the ganglioside rather than the membrane and ganglioside, and the interaction with ganglioside can be detected by fluorescence spectroscopy. In both the binding inhibition and fluorescence studies, luteinizing hormone recognizes an oligosaccharide sequence on the ganglioside molecule distinct from that of thyrotropin, human chorionic gonadotropin, and cholera toxin.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callMore From: Biochemical and Biophysical Research Communications
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
