Test Principle ImmunoCAP Tryptase

The technology is based on an extremely high total binding capacity, achieved through a high binding capacity per mg cellulose in combination with an optimal amount of cellulose in each solid phase. This ensures binding of all relevant antibodies, regardless of antibody affinity, still giving low non-specific binding.

The ImmunoCAP solid phase consists of a cellulose derivative enclosed in a capsule. The hydrophilic, highly branched polymer provides an ideal microenvironment for allergens, binding them irreversibly while maintaining their native structure.

The test is designed as a sandwich immunoassay.

Anti-tryptase, covalently coupled to the solid phase, reacts with the tryptase in the patient serum sample.
After washing, enzyme-labelled antibodies against tryptase are added to form a complex.
After incubation, unbound enzyme-anti-tryptase is washed away, and the bound complex is then incubated with a developing agent.
After stopping the reaction, the fluorescence of the eluate is measured. The fluorescence is directly proportional to the concentration of tryptase in the serum sample.


As in all diagnostic testing, the diagnosis is made by the physican based on both test results and the patient history.