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Adaptation of the dye-binding protein assay to microtiter plates

โœ Scribed by Margaret G. Redinbaugh; Wilbur H. Campbell


Publisher
Elsevier Science
Year
1985
Tongue
English
Weight
331 KB
Volume
147
Category
Article
ISSN
0003-2697

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โœฆ Synopsis


The dye-binding protein assay has been adapted for use with microtiter plates and a plate reader. The total volume of the assay was reduced to 0.2 ml, with equal volumes of sample. and diluted dye reagent being used. Because of the small volume, the assay is conservative of both protein sample and reagent. The use of microtiter plates allows the absorbance of samples to be read using a plate reader, markedly reducing the time needed for evaluating sample absorbances. This assay is quite sensitive, with a limit of less than 0.5 pg bovine serum albumin. In addition, the assay has been calibrated with homogeneous nitrate reductase. The response of nitrate reductase in the assay is about 70% of that of the standard protein, bovine serum albumin. The response of several other proteins was evaluated and the differences in response are discussed.


๐Ÿ“œ SIMILAR VOLUMES


Mechanism of Dye Binding in the Protein
โœ A.A. Waheed; K.Sridhar Rao; P.D. Gupta ๐Ÿ“‚ Article ๐Ÿ“… 2000 ๐Ÿ› Elsevier Science ๐ŸŒ English โš– 97 KB

Eosin B and eosin Y have been used to estimate micro- and submicrogram quantities of proteins respectively as shown in our previous reports. In the present study we describe the mechanism of eosin binding to proteins. At pH lower than 3.0 the absorbance of unbound dye is greatly reduced. After the d