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Recombinant Human Regulator of G-protein signaling 9 (RGS9)

ACP20715

Number
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High Purity LevelsPrecision and ReliabilityCustomization Options

Specifications


Cat.No ACP20715 Target NameRGS9
Target SynonymsPERRS; R9AP; Regulator of G protein signalling 9; Regulator of G-protein signaling 9; RGS9; RGS9_HUMAN; RGS9LFormLyophilized powder
Expression SystemCustom Production. Please inquire and provide the desire expression system.Expression Range1-674
Protein LengthFull length proteinPurity>85% (SDS-PAGE)
Storage Buffer5%-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.

Immunogen Information


Target SpeciesHumanUniprot IDO75916
Background Information
  • Uniprot Id

    O75916

  • Target Species

    Human

  • Target Name

    RGS9

  • Target Full Name

    Regulator of G-protein signaling 9

  • Target Function

    Inhibits signal transduction by increasing the GTPase activity of G protein alpha subunits thereby driving them into their inactive GDP-bound form. Binds to GNAT1. Involved in phototransduction; key element in the recovery phase of visual transduction.

  • Target Involvement

    Prolonged electroretinal response suppression (PERRS)

  • Target Subcellular Location

    [Isoform 3]: Membrane; Peripheral membrane protein.

  • Target Tissue Specificity

    Highly expressed in the caudate and putamen, lower levels found in the hypothalamus and nucleus accumbens and very low levels in cerebellum. Not expressed in globus pallidus or cingulate cortex. Isoform 2 is expressed predominantly in pineal gland and ret

  • Target Synonyms

    PERRS; R9AP; Regulator of G protein signalling 9; Regulator of G-protein signaling 9; RGS9; RGS9_HUMAN; RGS9L

  • Target Background

    This gene encodes a member of the RGS family of GTPase activating proteins that function in various signaling pathways by accelerating the deactivation of G proteins. This protein is anchored to photoreceptor membranes in retinal cells and deactivates G proteins in the rod and cone phototransduction cascades. Mutations in this gene result in bradyopsia. Multiple transcript variants encoding different isoforms have been found for this gene.

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