TSA multicolor immunofluorescence
Tyramide signal amplification (TSA) is an enzymatic method for the detection of target proteins using horseradish peroxidase (HRP) as a marker. Similar to the traditional immunohistochemical DAB color method, TSA technology also uses the second antibody of poly HRP, and contains the corresponding "color" step. In the reaction system, HRP catalyzes the addition of tyramine fluorescein substrate to produce an activated fluorescent substrate. This activated substrate can be covalently bound to tyrosine and other residues on the antigen to form a stable covalently bound tyramine fluorescein in the sample. This technology is widely used in TSA multi-color immunofluorescence experiment outsourcing projects.
Technical principle
Tyramide signal amplification (TSA) technology is an enzymatic detection method using horseradish peroxidase (HRP) to label the target protein. Similar to the regular immunohistochemical DAB color development method, TSA technology also uses the second antibody of poly HRP, and has the corresponding "color development" step. In the reaction system, HRP catalyzes the addition of tyramine fluorescein substrate to produce an active fluorescent substrate. This active substrate can be covalently bound to residues such as tyrosine on the antigen to form a stable covalently bound tyramine fluorescein on the sample. Next, the non-covalently bound primary antibody-secondary antibody-HRP complex was washed away using thermal repair, and a second round of incubation with another primary antibody-HRP secondary antibody was repeated. In each round of incubation, another tyramine fluorescein substrate can be exchanged to achieve multiple labeling.
Real Experimental Research Hundreds of Detection Experiments 6 Experimental Platforms









