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PDE10A2 TR-FRET Assay Kit

Phosphodiesterases (PDEs) play an important role in dynamic regulation of cAMP and cGMP signaling. PDE10A is a dual substrate PDE highly expressed in striatal medium spiny neurons. PDE10A inhibitors can improve the cognitive symptoms of schizophrenia, and exhibit potential therapeutic value for Huntington’s disease. PDE10A2 is located in cytosol, whereas PDE10A2 is a membrane-associated protein.ThePDE10A2TR-FRET Assay Kitis designed for identification of inhibitors of PDE10A2 using TR-FRET (Time Resolved Fluorescence Resonance Energy Transfer) technology. The assay is based on the generation of FAM-labeled nucleotide monophosphates by the phosphodiesterase. These phosphate groups bind to terbium-labeled nanoparticles, resulting in energy transfer from the terbium to the FAM, which emits a fluorescent signal at 520 nm. The change in fluorescent intensity can be easily measured using a fluorescence plate reader.Using this kit, only two simple steps on a microtiter plate are required for the PDE10A2 activity assay. First, the fluorescent-labeled cAMP is incubated with a sample containing PDE10A2 for 1 hour. Second, a binding agent and a terbium donor are added to the reaction mix and incubated for 1 hour. Then, fluorescence intensity can be measured using a fluorescence reader.Need us to run inhibitor screens or profile your compounds against PDE10A2? Check out ourPhosphodiesterase Screening Services.

Product Specifications

UniProt

Q9Y233

Applications

Great for screening small molecular inhibitors for drug discovery and HTS applications.

Format

Catalog #ComponentAmountStorage60100PDE10A2 recombinant enzyme1 µg-80°CAvoidfreeze/thawcycles!60200FAM-Cyclic-3′, 5′-AMP: 20 µM50 µl-80°C60393PDE assay buffer25 ml-20°C60394Tb donor50 µl-80°C60390Binding Agent200 µl+4°C78422Binding Buffer A20 ml+4°C78423Binding Buffer B20 ml+4°C79685Black, low binding NUNC microtiter pla1Room Temp.

Shipping Conditions

-80°C

Storage Conditions

At least 6 months from date of receipt, when stored as directed.

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