PDE7A Rabbit Polyclonal Antibody

Description: A polyclonal antibody for detection of PDE7A from Human, Mouse, Rat. This PDE7A antibody is for WB, ELISA. It is affinity-purified from rabbit serum by affinity-chromatography using the specific immunogenand is unconjugated. The antibody is produced in rabbit by using as an immunogen synthesized peptide derived from part region of human PDE7A protein

Description: Rabbit polyclonal PDE7A antibody

Description: Unconjugated Rabbit polyclonal to PDE7A

Description: The protein encoded by this gene belongs to the cyclic nucleotide phosphodiesterase (PDE) family, and PDE7 subfamily. This PDE hydrolyzes the second messenger, cAMP, which is a regulator and mediator of a number of cellular responses to extracellular signals. Thus, by regulating the cellular concentration of cAMP, this protein plays a key role in many important physiological processes. Alternatively spliced transcript variants encoding different isoforms have been described for this gene.

Description: Mouse polyclonal to PDE7A

Description: A cloning plasmid for the PDE7A gene.

Description: Human PDE7A1 GenBank Accession No. NM_002603), a.a. 121-end with N-terminal GST-tag, MW=66 kDa, expressed in a Baculovirus infected Sf9 cell expression system.

Description: The PDE7A Assay Kit is designed_x000D_for identification of PDE7A inhibitors using fluorescence polarization. The assay is_x000D_based on the binding of a fluorescent nucleotide monophosphate generated by PDE7A_x000D_to the binding agent. The key to the PDE7A_x000D_Assay Kit is the specific binding agent. Using this kit, only two simple steps on a_x000D_microtiter plate are required for PDE7A reactions. First, the fluorescently labeled cAMP_x000D_is incubated with a sample containing PDE7A for 1 hour. Second, a binding agent is_x000D_added to the reaction mix to produce a change in fluorescent polarization that can then_x000D_be measured using a fluorescence reader.

Description: The PDE7A Assay Kit is designed for identification of PDE7A inhibitors using_x000D_fluorescence polarization. The assay is based on the binding of a fluorescent nucleotide_x000D_monophosphate generated by PDE7A to the binding agent. PDE7A catalyzes the hydrolysis of_x000D_the phosphodiester bond in dye-labeled cyclic adenosine monophosphate (cAMP)._x000D_Nanoparticle beads selectively bind the phosphate group in the nucleotide product. This_x000D_increases the size of the nucleotide relative to unreacted cAMP. Since the degree of polarization_x000D_of a fluorophore is inversely related to its molecular rotation, dyes attached to the slowly-rotating_x000D_nucleotide-bead complexes will not have time to reorient and therefore will emit highly polarized_x000D_light. Conversely, dyes attached to the rapidly-rotating cyclic monophosphates will obtain_x000D_random orientations and emit light with low polarization. The key to the PDE7A Assay Kit is the specific_x000D_binding agent. Using this kit, only two simple steps on a microtiter plate are required for PDE7A_x000D_reactions. First, the fluorescently labeled cAMP is incubated with a sample containing PDE7A_x000D_for 1 hour. Second, a binding agent is added to the reaction mix to produce a change in_x000D_fluorescent polarization that can then be measured using a fluorescence reader.