scholarly journals Human chorionic gonadotropin. V. Tissue specificity of binding and partial characterization of soluble human chorionic gonadotropin-receptor complexes.

1975 ◽  
Vol 250 (10) ◽  
pp. 3837-3844
Author(s):  
R Bellisario ◽  
OP Bahl
Keyword(s):  
Chorionic Gonadotropin ◽  
Human Chorionic Gonadotropin ◽  
Tissue Specificity ◽  
Partial Characterization ◽  
Receptor Complexes ◽  
Gonadotropin Receptor ◽  
Specificity Of Binding

scholarly journals Endocrine pharmacology of reproduction (Report 40): Human chorionic gonadotropin receptor in the isolated rat uterus

1986 ◽  
Vol 40 ◽  
pp. 75
Author(s):  
Yoshiko Masubuchi ◽  
Taiichiro Ohno ◽  
Toshio Kumai ◽  
Masami Tanaka ◽  
Mitsuko Suetsuna ◽  
...  
Keyword(s):  
Chorionic Gonadotropin ◽  
Human Chorionic Gonadotropin ◽  
Rat Uterus ◽  
Gonadotropin Receptor ◽  
Isolated Rat

scholarly journals Evaluation of Nicked Human Chorionic Gonadotropin Content in Clinical Specimens by a Specific Immunometric Assay

1999 ◽  
Vol 45 (1) ◽  
pp. 68-77 ◽  
Author(s):  
Galina Kovalevskaya ◽  
Steven Birken ◽  
Tatsu Kakuma ◽  
John Schlatterer ◽  
John F O’Connor
Keyword(s):  
Chorionic Gonadotropin ◽  
Human Chorionic Gonadotropin ◽  
Normal Pregnancy ◽  
Physical Separation ◽  
Vitro Fertilization ◽  
Clinical Specimens ◽  
Reference Preparation ◽  
Ectopic Pregnancies

Abstract We report the development and characterization of an IRMA for the direct measurement of nicked human chorionic gonadotropin (hCGn) in blood and urine. hCGn derived from a reference preparation of hCG used as an immunogen elicits monoclonal antibodies (mAbs) with enhanced recognition of human luteinizing hormone epitopes. The most specific assay for pregnancy hCGn is an IRMA composed of one mAb to choriocarcinoma-derived hCGn (C5) and a second mAb developed from immunization with normal-pregnancy hCGn. This assay was used to evaluate hCGn profiles in normal, in vitro fertilization, Down syndrome, and ectopic pregnancies. In all pregnancies, hCGn was usually present in much lower concentrations than the non-nicked hCG isoform. Our results suggest that some form of physical separation from the overwhelming quantities of non-nicked hCG present in clinical specimens will be required before accurate immunochemical estimations of hCGn can be made.

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