Differences in humoral insulin-antibody response among inbred Lou/M rats and epitope presentation differences in ELISA and radioimmune titration

Diabetes ◽  
1989 ◽  
Vol 38 (7) ◽  
pp. 868-873 ◽  
Author(s):  
E. R. Arquilla ◽  
S. Edwards ◽  
B. R. McDougall ◽  
L. Mosqueda ◽  
D. P. Stenger
Diabetes ◽  
1989 ◽  
Vol 38 (7) ◽  
pp. 868-873 ◽  
Author(s):  
E. R. Arquilla ◽  
S. Edwards ◽  
B. R. McDougall ◽  
L. Mosqueda ◽  
D. P. Stenger

2003 ◽  
Vol 30 (3) ◽  
pp. 223-227 ◽  
Author(s):  
T. Battelino ◽  
N. Uršič-Bratina ◽  
V. Dolžan ◽  
M. Stopar-Obreza ◽  
P. Pozzilli ◽  
...  

2009 ◽  
Vol 47 (2) ◽  
pp. 131-135 ◽  
Author(s):  
Shilpa Oak ◽  
Thanh-Hien Thi Phan ◽  
Lisa K. Gilliam ◽  
Irl B. Hirsch ◽  
Christiane S. Hampe

Diabetes Care ◽  
1997 ◽  
Vol 20 (7) ◽  
pp. 1172-1175 ◽  
Author(s):  
M. Balsells ◽  
R. Corcoy ◽  
D. Mauricio ◽  
J. Morales ◽  
A. Garcia-Patterson ◽  
...  

Author(s):  
Burton B. Silver ◽  
Ronald S. Nelson

Some investigators feel that insulin does not enter cells but exerts its influence in some manner on the cell surface. Ferritin labeling of insulin and insulin antibody was used to determine if binding sites of insulin to specific target organs could be seen with electron microscopy.Alloxanized rats were considered diabetic if blood sugar levels were in excess of 300 mg %. Test reagents included ferritin, ferritin labeled insulin, and ferritin labeled insulin antibody. Target organs examined were were diaphragm, kidney, gastrocnemius, fat pad, liver and anterior pituitary. Reagents were administered through the left common carotid. Survival time was at least one hour in test animals. Tissue incubation studies were also done in normal as well as diabetic rats. Specimens were fixed in gluteraldehyde and osmium followed by staining with lead and uranium salts. Some tissues were not stained.


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