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Recombinant Human Rhodopsin (RHO), Truncated

ACP03759

Number
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Specifications


Cat.No ACP03759 Target NameRHO
FormLiquid or Lyophilized powderExpression SystemE.coli
Expression Range1-36AAMol Weight20.2kDa
Protein LengthPartialPurityGreater than 90% as determined by 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 IDP08100
Background Information
  • Uniprot Id

    P08100

  • Target Species

    Human

  • Target Name

    RHO

  • Target Full Name

    Rhodopsin

  • Target Function

    Photoreceptor required for image-forming vision at low light intensity. Required for photoreceptor cell viability after birth. Light-induced isomerization of the chromophore 11-cis-retinal to all-trans-retinal triggers a conformational change that activates signaling via G-proteins. Subsequent receptor phosphorylation mediates displacement of the bound G-protein alpha subunit by the arrestin SAG and terminates signaling.

  • Target Involvement

    Retinitis pigmentosa 4 (RP4); Night blindness, congenital stationary, autosomal dominant 1 (CSNBAD1)

  • Target Subcellular Location

    Membrane; Multi-pass membrane protein. Cell projection, cilium, photoreceptor outer segment.

  • Target Protein Families

    G-protein coupled receptor 1 family, Opsin subfamily

  • Target Tissue Specificity

    Rod shaped photoreceptor cells which mediate vision in dim light.

  • Target Research Area

    Signal Transduction

  • Target Synonyms

    CSNBAD1; MGC138309; MGC138311; OPN 2; OPN2; opsd; OPSD_HUMAN; opsin 2; Opsin 2 rod pigment; Opsin-2; Opsin2; Retinitis Pigmentosa 4; Retinitis pigmentosa 4 autosomal dominant; RHO; Rhodopsin; RP 4; RP4

  • Target Background

    The protein encoded by this gene is found in rod cells in the back of the eye and is essential for vision in low-light conditions. The encoded protein binds to 11-cis retinal and is activated when light hits the retinal molecule. Defects in this gene are a cause of congenital stationary night blindness.

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