JBC Origene Your Gene Company

HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Gospodarowicz, D.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Gospodarowicz, D.
Social Bookmarking
 Add to CiteULike   Add to Complore   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Reddit   Add to Technorati  
What's this?

Single Step Purification of Ovine Luteinizing Hormone by Affinity Chromatography

Denis Gospodarowicz 1

From the 1 From The Salk Institute for Biological Studies, Post Office Box 1809, San Diego, California 92112

Affinity chromatography has been applied to the problem of specifically removing luteinizing hormone from sera used to supplement tissue culture media. Horse or fetal calf sera, passed through a column of an anti-luteinizing hormone immunoglobulin fraction linked covalently to agarose, were specifically depleted in their content of luteinizing hormone as seen by radioimmunoassay and by their effect on cultures of ovarian cells dependant on luteinizing hormone for their growth.

Affinity chromatography has also been applied to the one step isolation of luteinizing hormone from a partially purified or crude extract of ovine pituitary glands. Partially purified extracts or crude extracts of pituitary glands, passed through a column of an anti-luteinizing hormone immunoglobulin fraction linked covalently to agarose, were depleted in their luteinizing hormone content. Elution of the column by 6 m guanidine HCl pH 1.5 resulted in the recovery of the hormone which was further characterized by chemical and biological analysis as well as its electrophoretic pattern. It was demonstrated that affinity chromatography can be used to isolate preparations of highly homogeneous ovine luteinizing hormone in one step.

Submitted on January 14, 1972


Add to CiteULike CiteULike   Add to Complore Complore   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati    What's this?


This article has been cited by other articles:


Home page
ScienceHome page
R. Starkey, S Cohen, and D. Orth
Epidermal growth factor: identification of a new hormone in human urine
Science, September 5, 1975; 189(4205): 800 - 802.
[Abstract] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 All ASBMB Journals   Molecular and Cellular Proteomics 
 Journal of Lipid Research   ASBMB Today 
Copyright © 1972 by the American Society for Biochemistry and Molecular Biology.