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Nowadays most of the accepted assays for protein are spectrophotometric such as the Lowry, Coomassie brilliant blue (CBB), bromophenol blue and bromocresol green methods. However, they have some disadvantages in aspects of sensitivity, selectivity, stability and operation. For example, the Lowry, bromophenol blue and bromocresol green methods are insensitive and have serious interference from coexisting substances. The CBB assay, although sensitive, is inconvenient in application due to the non-linear calibration graph and limited stability of the CBB–protein complex.