The human serum proteome: Display of nearly 3700 chromatographically separated protein spots on two-dimensional electrophoresis gels and identification of 325 distinct proteins

PROTEOMICS ◽  
2003 ◽  
Vol 3 (7) ◽  
pp. 1345-1364 ◽  
Author(s):  
Rembert Pieper ◽  
Christine L. Gatlin ◽  
Anthony J. Makusky ◽  
Paul S. Russo ◽  
Courtney R. Schatz ◽  
...  
1992 ◽  
Vol 13 (1) ◽  
pp. 743-746 ◽  
Author(s):  
Luca Bini ◽  
Barbara Magi ◽  
Carla Cellesi ◽  
Aldo Rossolini ◽  
Vitaliano Pallini

1979 ◽  
Vol 7 (5) ◽  
pp. 1089-1090 ◽  
Author(s):  
ANNE E. HUGHES ◽  
W. SIDNEY B. LOWRY ◽  
J. ALAN HILL ◽  
R. JEREMY H. DAVIES

1995 ◽  
Vol 16 (1) ◽  
pp. 1190-1192 ◽  
Author(s):  
Barbara Magi ◽  
Barbara Marzocchi ◽  
Luca Bini ◽  
Carla Cellesi ◽  
Aldo Rossolini ◽  
...  

1982 ◽  
Vol 28 (4) ◽  
pp. 824-827 ◽  
Author(s):  
T Manabe ◽  
E Hayama ◽  
T Okuyama

Abstract In this technique, in which no denaturing agent is used, proteins in human serum, cerebrospinal fluid, and urine are separated by isoelectric focusing in cylindrical 40 g/L polyacrylamide gels of capillary size (1.3 x 35 mm) for 40 min, followed by electrophoresis in 40--170 g/L polyacrylamide linear gradient gel, with use of 38 x 35 x 1 mm slab gel, for 1 h. Only 2 microL of untreated human serum is required to obtain clear protein-distribution patterns, made visible by Coomassie Blue staining. By use of silver staining, proteins in unconcentrated cerebrospinal fluid can be made visible. An apparatus we devised for microscale two-dimensional electrophoresis enables us to analyze eight protein samples simultaneously.


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