Coomassie brilliant blue G-250 dye-binding technique for determination of autolytic protein breakdown in Euglena gracilis and comparison to other methods of autolysis measurement

1986 ◽  
Vol 153 (2) ◽  
pp. 242-250 ◽  
Author(s):  
Rainald Krauspe ◽  
Angelika Scheer
1985 ◽  
Vol 151 (2) ◽  
pp. 571-574 ◽  
Author(s):  
R.A. Asryants ◽  
I.V. Duszenkova ◽  
N.K. Nagradova

1987 ◽  
Vol 33 (4) ◽  
pp. 577-578 ◽  
Author(s):  
T Marshall ◽  
K M Williams

Abstract We investigated the influence of assay protocol upon results of Coomassie Brilliant Blue protein dye-binding assays for urinary protein. Sensitivity and working range for, and linearity of response (including dilution dependence) of, three standard assays and four micro assays to bovine albumin, gamma-globulin, and urine are compared. The Read and Northcote standard assay (Anal Biochem 1981; 116:53-64) appears to be the method of choice.


1989 ◽  
Vol 35 (10) ◽  
pp. 2127-2129 ◽  
Author(s):  
Y Bergqvist ◽  
L Karlsson ◽  
L Fohlin

Abstract This simple method of centrifugal analysis for total protein in human breast milk is based on the change in the wavelength of the absorbance maximum of Coomassie Brilliant Blue G-250 when the dye is bound to protein. Within-run and between-day CVs were 3.8% and 4.8%, respectively. Compared with a micro-Kjeldahl method for determination of total nitrogen, the coefficient of correlation was 0.99.


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