Starch-gel Electrophoresis of Pig Serum Proteins

Nature ◽  
1963 ◽  
Vol 197 (4873) ◽  
pp. 1201-1201 ◽  
Author(s):  
R. K. SCOPES
1966 ◽  
Vol 12 (4) ◽  
pp. 181-186 ◽  
Author(s):  
Clyde A Dubbs

Abstract Several significant effects of ultrasonic treatment on human serum cholinesterase and aminopeptidase isoenzymes and on other serum proteins have been found by starch gel electrophoresis. The selective activation of one cholinesterase isoenzyme is especially striking. These effects must be considered when ultrasonic treatment is used for the extraction of intracellular enzymes. When the effects are appreciated, ultrasonics should provide a valuable tool for isoenzyme research.


1965 ◽  
Vol 43 (4) ◽  
pp. 459-461 ◽  
Author(s):  
M. Latifi ◽  
K. D. Shamloo ◽  
A. Amin

Paper and starch-gel electrophoresis of serum proteins of several species and subspecies of poisonous and nonpoisonous snakes of Iran have been investigated. The patterns obtained, especially by means of the starch-gel method, are characteristic for each species. Electrophoretic patterns of samples of serum from different individuals of the same species were very similar.


1961 ◽  
Vol 236 (7) ◽  
pp. 2005-2008
Author(s):  
George H. Beaton ◽  
Anne E. Selby ◽  
Margaret J. Veen ◽  
Audrey M. Wright

1966 ◽  
Vol 12 (9) ◽  
pp. 596-605 ◽  
Author(s):  
Lena A Lewis

Abstract A modification of the starch-gel electrophoresis technic of Smithies is presented,which enables quantitation of the resolved fractions to be carried out with little equipment other than that used for paper electrophoretic fractionation of proteins.A sheet of plastic (Stabilene film) wrapped around a kymograph type drum is evenly coated with starch-gel. The sheet is suspended in an "open strip" Durrum type cell and electrophoresis carried out. After staining with suitable stain to demonstrate proteins, lipids, or other components, the patterns are scanned in a photoelectric densitometer. Results obtained with this procedure show good reproducibility when fractionating solutions of hemoglobin and serum proteins.


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