Bicinchoninic Acid Kit
Protein Determination is one of the most common operations performed in biochemical research. The principle of the bicinchoninic acid (BCA) assay is similar to the Lowry procedure, in that both rely on the formation of a Cu2+-protein complex under alkaline conditions, followed by reduction of the Cu2+ to Cu1+. The amount of reduction is proportional to the protein present. It has been shown that cysteine, cystine, tryptophan, tyrosine, and the peptide bond are able to reduce Cu2+ to Cu1+. BCA forms a purple-blue complex with Cu1+ in alkaline environments, thus providing a basis to monitor the reduction of alkaline Cu2+ by proteins at absorbance maximum 562 nm. The BCA assay is more sensitive and applicable than either Biuret or Lowry procedures. In addition, it has less variability than the Bradford assay. The BCA assay has many advantages over other protein determination techniques:
- The color complex is stable.
- There is less susceptibility to detergents.
- It is applicable over a broad range of protein concentrations.
Bicinchoninic Acid Solution
4% (w/v) CuSO 4 • 5H2O Solution
Protein Standard Solution
BCA Protein Compatibility Chart
||Bicinchoninic Acid Kit for Protein Determination
||Bicinchoninic Acid Solution
||Bicinchoninic Acid Disodium Sal
||Copper (II) Sulfate Solution
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