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Recombinant Human Rhodopsin kinase (GRK1)

ACP17807

Number
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High Purity LevelsPrecision and ReliabilityCustomization Options

Specifications


Cat.No ACP17807 Target NameGRK1
Target SynonymsEC=2.7.11.14; G protein-coupled receptor kinase 1; GPRK1; Grk1; Rhodopsin kinase; RHOK; RK; RK_HUMANFormLyophilized powder
Expression SystemCustom Production. Please inquire and provide the desire expression system.Expression Range1-560
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 IDQ15835
Background Information
  • Uniprot Id

    Q15835

  • Target Species

    Human

  • Target Name

    GRK1

  • Target Full Name

    Rhodopsin kinase GRK1

  • Target Function

    Retina-specific kinase involved in the signal turnoff via phosphorylation of rhodopsin (RHO), the G protein- coupled receptor that initiates the phototransduction cascade. This rapid desensitization is essential for scotopic vision and permits rapid adaptation to changes in illumination. May play a role in the maintenance of the outer nuclear layer in the retina.

  • Target Involvement

    Night blindness, congenital stationary, Oguchi type 2 (CSNBO2)

  • Target Subcellular Location

    Membrane; Lipid-anchor. Cell projection, cilium, photoreceptor outer segment.

  • Target Protein Families

    Protein kinase superfamily, AGC Ser/Thr protein kinase family, GPRK subfamily

  • Target Tissue Specificity

    Retinal-specific. Expressed in rods and cones cells.

  • Target Synonyms

    EC=2.7.11.14; G protein-coupled receptor kinase 1; GPRK1; Grk1; Rhodopsin kinase; RHOK; RK; RK_HUMAN

  • Target Background

    This gene encodes a member of the guanine nucleotide-binding protein (G protein)-coupled receptor kinase subfamily of the Ser/Thr protein kinase family. The protein phosphorylates rhodopsin and initiates its deactivation. Defects in GRK1 are known to cause Oguchi disease 2 (also known as stationary night blindness Oguchi type-2).

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