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137329 PDE1B, BioAssay™ Kit (Calcium/Calmodulin-dependent 3',5'-cyclic Nucleotide Phosphodiesterase 1B, Cam-PDE 1B, 63kD Cam-PDE, PDE1B1, PDES1B)

Specifications
References
Brand
BioAssay™
Kit Type
Assay
Tests
100
Detection Method
Colorimetric/Fluorescent
EU Commodity Code
38220000
Shipping Temp
Blue Ice
Storage Temp
-20°C

Phosphodiesterases (PDEs) play an important role in dynamic regulation of cAMP and cGMP signaling. PDE1B is a calcium-dependent cyclic nucleotide phosphodiesterase that is highly expressed in the striatum. It plays a physiological role in the central nervous system, and PDE1B activity has been linked to impaired cognition and spatial learning. The PDE1B Assay Kit is designed for identification of PDE1B inhibitors using fluorescence polarization. The assay is based on the binding of a fluorescent nucleotide monophosphate generated by PDE1B to the binding agent.

Intended Use
Designed for identification of PDE1B inhibitors using fluorescence polarization.
Test Principle
The PDE1B inhibitor screening assay kit comes in a convenient 96-well format, including purified PDE1B enzyme, fluorescently labeled PDE1B substrate (cAMP), binding agent, and PDE assay buffer for 100 enzyme reactions. The key to the PDE1B Assay Kit is the specific binding agent. Using this kit, only two simple steps on a microtiter plate are required for PDE1B reactions. First, the fluorescently labeled cAMP is incubated with a sample containing PDE1B for 1 hour. Second, a binding agent is added to the reaction mix to produce a change in fluorescent polarization that can then be measured using a fluorescence reader equipped for the measurement of fluorescence polarization.
Kit Components
PDE1B: 1x1ug FAM-Cyclic-3’, 5’-AMP: 20uM: 1x50ul PDE assay buffer: 1x12ml Binding Agent: 1x100ul Binding Agent Diluent: 1x10ml Black, low binding NUNC black microtiter plate: 1 plate
Storage and Stability
Store other components at 4°C. Stable for at least 6 months For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap.
References
1. Siuciak JA, et al. (2007) Neuropharmacology 53(1):113-24.
USBio References
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