Colorimetric Micromethod for Protein Determination with Erythrosin B
β Scribed by H.S. Soedjak
- Book ID
- 102965137
- Publisher
- Elsevier Science
- Year
- 1994
- Tongue
- English
- Weight
- 547 KB
- Volume
- 220
- Category
- Article
- ISSN
- 0003-2697
No coin nor oath required. For personal study only.
β¦ Synopsis
Reaction of erythrosin B with proteins results in a stable, highly colored chromophore with an absorbance maximum at (545 \mathrm{~nm}). This is the basis for a new quantitative determination method of proteins in solution. The assay can be performed at room temperature, but is faster and more sensitive at (90-95^{\circ} \mathrm{C}). The erythrosin assay is characterized by (i) stable dye-protein color, (ii) high sensitivity ((2-14 \mu \mathrm{g} / \mathrm{ml}) protein), (iii) short reaction time (1.5-2 (\min) at (90-95^{\circ} \mathrm{C}) ), (iv) good reproducibility, (v) limited interference by common reagents, and (vi) low protein-to-protein variability. Thus, the erythrosin assay can be useful for routine analytical purposes and may overcome some of the limitations of other currently employed assays. c 1994 Academic Press, Inc.
π SIMILAR VOLUMES
A method of determination of protein based on the measurement of complexed Ag+ and A&l absorbed on the macromolecules is described. This reaction is carried out in the presence of chloride ions and detergents (Triton X-100 or SDS) in alkaline solution. The silver ions are detected with dithizone. Wi