Routine determination of enzyme kinetics using Plate reader

1991 ◽  
Vol 38 (4) ◽  
pp. 434-437 ◽  
Author(s):  
F. Galgani ◽  
Y. Cadiou ◽  
G. Bocquene
Keyword(s):  
2011 ◽  
Vol 699 (1) ◽  
pp. 107-112 ◽  
Author(s):  
Nedime Dürüst ◽  
Mark E. Meyerhoff ◽  
Nazangül Ünal ◽  
Sibel Naç

2010 ◽  
Vol 93 (1) ◽  
pp. 89-96 ◽  
Author(s):  
Mark J Payne ◽  
William Jeffrey Hurst ◽  
David A Stuart ◽  
Boxin Ou ◽  
Ellen Fan ◽  
...  

Abstract A simple, specific, high-throughput colorimetric method based on the reaction of 4-dimethylaminocinnamaldehyde (DMAC) with flavan-3-ols was developed to determine total procyanidins in selected cacao-based products. Extracts of defatted samples were dispensed into a 96-well plate and reacted with DMAC. The absorbance of the reaction products was measured at 640 nm and compared to commercially available procyanidin B2 as a standard. The use of the 96-well plates and a plate reader dramatically improved sample throughput. A standard protocol was established and used for further studies. The calibration was found to be linear from 1100 ppm. The DMAC reagent reacted relatively specifically to (–)-epicatechin, (+)-catechin, epigallocatechin, gallocatechin, the gallates of catechin, epicatechin, gallocatechin, and epigallocatechin, oligomeric procyanidins of cocoa up to n = 4, and A-type procyanidins. Little or no reaction occurred with cyanidins and representative compounds of phenolic acids, flavones, flavanones, flavonols, anthocyanidins, isoflavones, and stilbenes. Sample precision studies were carried out on 10 different test materials over several weeks, and yielded RSD values of 4.0 to 9.5%. The method was ring-tested in three laboratories using blinded test materials including cocoa beans, cocoa powder, chocolate liquor, dark chocolate, and milk chocolate. There was excellent agreement of the results between laboratories.


1994 ◽  
Vol 77 (5) ◽  
pp. 1308-1313 ◽  
Author(s):  
Elizabeth R Tor ◽  
Dirk M Holstege ◽  
Francis D Galey

Abstract A rapid method is described for the quantitative determination of cholinesterase activity in large batches of blood and brain samples. The technique is an adaptation of the Ellman procedure for a 96-well microtiter plate reader. Ten samples can be analyzed simultaneously in 5 min, with all calculations, including statistical analysis, done automat- ically. The method detection limit is 0.1 μM/mL/min for blood and 0.1 μM/g/min for brain samples. The procedure has been applied to the routine analyses of samples presented to the veterinary diagnostic laboratory. Method performance, quality control, and normal ranges of cholinesterase activity in live- stock and other animals are described.


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