scholarly journals Why does Coomassie Brilliant Blue R interact differently with different proteins? A partial answer.

1985 ◽  
Vol 260 (18) ◽  
pp. 9976-9980 ◽  
Author(s):  
M Tal ◽  
A Silberstein ◽  
E Nusser
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.


2016 ◽  
Vol 869 ◽  
pp. 765-767 ◽  
Author(s):  
Layane Rodrigues Almeida ◽  
João Sammy Nery Souza ◽  
Edson Cavalcanti Silva Filho ◽  
Josy Anteveli Osajima

The presence of organic pollutants, which cannot be eliminated by conventional processes of primary and secondary treatment, can be problematic. Photocatalytic processes offer an efficient breakdown of organic pollutants into non-toxic compounds such as CO2 and H2O. This paper proposes the use of the titanium dioxide embedded in palygorskite as a photoactive material in the degradation of cationic dye, Coomassie Brilliant Blue. The system was irradiated using UV light for a maximum time of 120 minutes. The concentration of the dye used was 1.0x10-4 mol L-1 in 0.5 g L-1 of the photoactive material. The kinetics of the system was monitored by UV-Vis spectrophotometry. In 120 minutes of radiation, the process of photocatalysis reduced the initial concentration of the Coomassie Brilliant Blue dye in half.


2017 ◽  
Vol 86 ◽  
pp. 213-217 ◽  
Author(s):  
Naveed A. Shad ◽  
Mehvish Zahoor ◽  
Khizra Bano ◽  
Sadia Z. Bajwa ◽  
Nasir Amin ◽  
...  

2015 ◽  
Vol 3 (3) ◽  
pp. 373-380 ◽  
Author(s):  
Shiv Kumar Verma ◽  
Anand Kumar ◽  
Moti Lal ◽  
Mira Debnath

In this study, based on colony morphology characteristics, a total of 19 fungal endophytes were isolated from root of Calotropis Procera a traditional Indian medicinal plant. All fungal isolates were screened for their dye degradation ability. The dyes used as test dyes were Rose Bengal (RB), azo dye Methyl Red (MR), Coomassie Brilliant Blue (CBB) and Methylene Blue (MB) and the concentration of each dye in the experiment was kept 100mg/L. Among the 19 fungal endophytic isolates (CPR1-CPR19), only one isolate CPR4 showed strong dye decolourization capability against all the four test dye. Dye decolourization ability by the isolate CPR4 was determined to be 97.4%, 87%, 65% and 45% for Rose Bengal (RB), Methyl Red (MR), Coomassie Brilliant Blue (CBB) and Methylene Blue (MB) respectively. Complete colour decolourization was observed with rose Bengal followed by Methyl Red. Glucose minimal medium was used for liquid and solid culture of fungal isolates. Fungal biomass production in the presence of four test dye was studied and compare with control culture of fungal endophytes. Effect of temperature, pH, stationary and agitation conditions on dye degradation was also studied.Int J Appl Sci Biotechnol, Vol 3(3): 373-380 


Health ◽  
2009 ◽  
Vol 01 (03) ◽  
pp. 146-151
Author(s):  
Yajun Wu ◽  
Ying Chen ◽  
Bin Wang ◽  
Haiyan Wang ◽  
Fei Yuan ◽  
...  

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