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| Cat.No | ACP15752 | Target Name | RGS9BP |
|---|---|---|---|
| Target Synonyms | RGS9BP; R9AP; Regulator of G-protein signaling 9-binding protein; RGS9-anchoring protein | Form | Lyophilized powder |
| Expression System | Custom Production. Please inquire and provide the desire expression system. | Protein Length | Partial |
| Purity | >85% (SDS-PAGE) | Storage Buffer | 5%-50% glycerol. Lyophilized powder form: the buffer before lyophilization is Tris/PBS-based buffer, 6% Trehalose, Liquid form: default storage buffer is Tris/PBS-based buffer, pH 8.0. |
| Target Species | Human | Uniprot ID | Q6ZS82 |
|---|
Uniprot Id
Q6ZS82
Target Species
Human
Target Name
RGS9BP
Target Full Name
Regulator of G-protein signaling 9-binding protein
Target Function
Regulator of G protein-coupled receptor (GPCR) signaling in phototransduction. Participates in the recovery phase of visual transduction via its interaction with RGS9-1 isoform. Acts as a membrane-anchor that mediates the targeting of RGS9-1 to the photoreceptor outer segment, where phototransduction takes place. Enhances the ability of RGS9-1 to stimulate G protein GTPase activity, allowing the visual signal to be terminated on the physiologically time scale. It also controls the proteolytic stability of RGS9-1, probably by protecting it from degradation.
Target Involvement
Prolonged electroretinal response suppression (PERRS)
Target Subcellular Location
Membrane; Single-pass type IV membrane protein.
Target Protein Families
RGS7BP/RGS9BP family
Target Synonyms
RGS9BP; R9AP; Regulator of G-protein signaling 9-binding protein; RGS9-anchoring protein
Target Background
The protein encoded by this gene functions as a regulator of G protein-coupled receptor signaling in phototransduction. Studies in bovine and mouse show that this gene is expressed only in the retina, and is localized in the rod outer segment membranes. This protein is associated with a heterotetrameric complex, specifically interacting with the regulator of G-protein signaling 9, and appears to function as the membrane anchor for the other largely soluble interacting partners. Mutations in this gene are associated with prolonged electroretinal response suppression (PERRS), also known as bradyopsia.
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