Double antibody solid-phase radioimmunoassay for staphylococcal enterotoxin A

1977 ◽  
Vol 4 (2) ◽  
pp. 137-143 ◽  
Author(s):  
S. Lindroth ◽  
A. Niskanen
1973 ◽  
Vol 25 (5) ◽  
pp. 774-777 ◽  
Author(s):  
William S. Collins ◽  
Anna D. Johnson ◽  
Joseph F. Metzger ◽  
Reginald W. Bennett

1973 ◽  
Vol 25 (5) ◽  
pp. 774-777
Author(s):  
William S. Collins ◽  
Anna D. Johnson ◽  
Joseph F. Metzger ◽  
Reginald W. Bennett

1975 ◽  
Vol 30 (4) ◽  
pp. 700-701
Author(s):  
Joann A. Bukovic ◽  
Howard M. Johnson

Author(s):  
AC Lovesey

The measurement of plasma levels of human follicle-stimulating hormone (FSH) has proved to be of value for the study of the hypothalamic-hypophyseal-gonadal axis, greatly facilitating the diagnosis and management of problems relating to the menopause and infertility. In the present work a solid-phase radioimmunoassay for human FSH has been developed. This system is characterised by high precision, is economical, and is considerably faster to operate than conventional double antibody systems used in the hospital assay service. Reference values for plasma FSH in various endocrine states are recorded and discussed.


1973 ◽  
Vol 40 (2) ◽  
pp. 235-245 ◽  
Author(s):  
I. C. Hart

SummaryThe development of a rapid, highly sensitive double antibody–solid phase (DASP) radioimmunoassay for ovine/caprine prolactin is described. The assay was applied to the measurement of basal levels of prolactin in the blood of 4 anoestrous lactating female, 4 anoestrous virgin female and 4 castrated male goats. For several hours after milking there was a chronic gradually decreasing release of prolactin in the lactating goats, such that the circulating levels of prolactin were, for 14–16 h of the day, at a much higher level than those in the virgin female or castrated male goats. The basal levels of prolactin in the castrated male goats (87–200ng/ml) were somewhat higher than those in the virgin females (47–77ng/ml). The effects of feeding and stress on prolactin levels are discussed.


1981 ◽  
Vol 27 (1) ◽  
pp. 39-42 ◽  
Author(s):  
V T Kung ◽  
P M Weber ◽  
L V dos Remedios

Abstract We describe a double-antibody radioimmunoassay for antimicrosomal antibodies in serum. Antigen in centrifuged pellets of microsome is solubilized by treatment with sodium deoxycholate solution and radiolabeled (125I] by the Chloramine T method. A 10-microL aliquot of human serum or antimicrosomal antibody standard is incubated overnight at room temperature with 125I-labeled microsome. Bound radiolabeled microsome is separated by precipitation with goat antihuman IgG antiserum. The percentage of 125I-labeled microsome bound by each serum is calculated, and its concentration of antimicrosomal antibody interpolated from a standard curve. The prevalence of abnormal antimicrosomal antibody was 16% in a self-referred asymptomatic or not acutely ill group of patients having a periodic multiphasic health examination. Values for patients with certain thyroid diseases generally agreed with other published data. We conclude that our assay is sensitive, precise, and accurate, and is more efficient for routine measurement of antimicrosomal antibody than the currently used solid-phase radioimmunoassay.


Kanzo ◽  
1974 ◽  
Vol 15 (7) ◽  
pp. 427-432
Author(s):  
Shinichi KAKUMU ◽  
Shozo ITO ◽  
Sumihiko OKUYAMA ◽  
Seikichi INADA ◽  
Katsuhiko TAGO

1971 ◽  
Vol 22 (5) ◽  
pp. 837-841
Author(s):  
Howard M. Johnson ◽  
Joann A. Bukovic ◽  
Peter E. Kauffman ◽  
J. T. Peeler

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