scholarly journals Sodium dodecyl sulfate-agarose gel electrophoresis of urinary proteins: application to multiple myeloma

1998 ◽  
Vol 44 (6) ◽  
pp. 1191-1197 ◽  
Author(s):  
Thierry Le Bricon ◽  
Danielle Erlich ◽  
Djaouida Bengoufa ◽  
Michelle Dussaucy ◽  
Jean-Pierre Garnier ◽  
...  

Abstract We evaluated a new sodium dodecyl sulfate-agarose gel electrophoresis (SDS-AGE) for urinary protein analysis in patients with multiple myeloma (MM; n = 47; ages, 62 ± 2 years, mean ± SE). Abnormal proteinuria (mean = 1872 ± 360 mg/24 h) was present in 95% of the samples; 75% of the patients had some sign of renal dysfunction (glomerular and/or tubular) according to their SDS-AGE pattern. A band suggesting Bence Jones proteinuria (BJP) was detected in 40 vs 33 specimens by routine AGE. Immunofixation identified BJP in 38 patients; the calculated sensitivity of SDS-AGE for BJP was 97%. Excellent correlation (P <0.0001) was obtained with routine AGE (r = 0.994) and immunonephelometry (r = 0.963) for light chain quantification. SDS-AGE allows easy evaluation of renal dysfunction and shows high sensitivity for BJP detection. In a specialized laboratory, it is useful for following the progress of MM patients through the semiquantification of BJP.

2003 ◽  
Vol 47 (3) ◽  
pp. 91-97 ◽  
Author(s):  
Kayo Yokomizo ◽  
Yuka Azuma ◽  
Kumi Onose ◽  
Keiichiro Okabe ◽  
Kiyoko Shiba ◽  
...  

1986 ◽  
Vol 7 (11) ◽  
pp. 496-505 ◽  
Author(s):  
Hans-Walter Schiwara ◽  
Thomas Hebell ◽  
Hartmut Kirchherr ◽  
Wilhelm Postel ◽  
Johannes Weser ◽  
...  

1986 ◽  
Vol 32 (5) ◽  
pp. 811-815 ◽  
Author(s):  
J M Perini ◽  
B Dehon ◽  
T Marianne ◽  
A Klein ◽  
P Roussel

Abstract Immunoblots of several urinary low-molecular-mass proteins can be very useful in investigations of pathological proteinuria. However, use of certain commercial antisera in such procedures leads to artifacts corresponding to nonspecific bands; e.g., immunoglobulins from nonimmunized rabbit serum may bind to human urinary proteins, and this binding is not inhibited by Triton X-100. We have developed a procedure to improve the specificity of detection of urinary low-Mr proteins separated by sodium dodecyl sulfate-polyacrylamide gel electrophoresis, by immunoblotting with commercial antisera: we treat the protein blot with a mixture of mercaptoethanol and sodium dodecyl sulfate before incubation with the first antiserum. This allows direct use of commercial antisera without prior absorption of contaminating antibodies.


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