-
-
Overview
-
The DNase Activity Detection Kit (Fluorescent Labeling Method) uses a new type of DNA substrate, which is labeled with a fluorescent reporter group molecule at one end and a quencher group at the other end. In the absence of DNase, the physical proximity of the quencher group will quench the fluorescence in the fluorescent reporter group to an extremely low level. When DNase is present, the DNA substrate is hydrolyzed, and the fluorescent reporter group and the quencher group are spatially separated in the solution, which causes the fluorescent reporter group to emit bright fluorescence when excited by light of the appropriate wavelength, which can be detected by a multifunctional microplate reader (including a fluorescence module) and a fluorescent quantitative PCR instrument.
Please contact us at for specific academic pricing.
-
- Properties
- Applications
-
Overview