Standardization of the Coomassie Blue method for cerebrospinal fluid proteins.
- 1 November 1978
- journal article
- research article
- Published by Oxford University Press (OUP) in Clinical Chemistry
- Vol. 24 (11), 1931-1933
- https://doi.org/10.1093/clinchem/24.11.1931
Abstract
Coomassie Brilliant Blue G-250 can be used to quantitatively determine proteins in cerebrospinal fluid. When the dye combines with protein, the absorption maximum of the dye shifts. The dye-protein color forms almost instantaneously and is stable for at least 1 h. The procedure is also insensitive to changes in temperature in the range of 20--30 degrees C. The absorptivities of the dye complexes with human albumin or globulin differ, thus a pure albumin or pure globulin standard is unsuitable; a standard containing 70% albumin and 30% globulins is the most appropriate for this application. A bichromatic approach to standardization increases the range of linearity of a calibration curve. The method gives values that are about 9% higher than a sodium sulfate-sulfosalicylic turbidimetric procedure for cerbrospinal fluid proteins.This publication has 5 references indexed in Scilit:
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- Characteristics of statistical parameters used to interpret least-squares results.Clinical Chemistry, 1978
- An evaluation of the Coomassie brilliant blue G-250 dye-binding method for quantitative protein determinationAnalytical Biochemistry, 1977
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- A Rapid and Sensitive Method for the Quantitation of Microgram Quantities of Protein Utilizing the Principle of Protein-Dye BindingAnalytical Biochemistry, 1976