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Human RPE65 Protein, His Tag

This product is still under development. Please contact us if you have interest in this product. We will accelerate the development process accordingly and reserve this product for you as request.
  • Synonym
    BCO3, LCA2, RP20, mRPE65, p63, rd12, sRPE65
  • Source
    Human RPE65 Protein, His Tag(RP5-H52H3) is expressed from human 293 cells (HEK293). It contains AA Ser 2 - Ser 533 (Accession # Q16518).
    Predicted N-terminus: His
  • Molecular Characterization
    RPE65 Structure

    This protein carries a polyhistidine tag at the C-terminus

    The protein has a calculated MW of 62.8 kDa.

  • Formulation

    Please contact us for detailed information.

    Contact us for customized product form or formulation.

  • Reconstitution

    Please see Certificate of Analysis for specific instructions.

    For best performance, we strongly recommend you to follow the reconstitution protocol provided in the CoA.

  • Storage

    For long term storage, the product should be stored at lyophilized state at -20°C or lower.

    Please avoid repeated freeze-thaw cycles.

    This product is stable after storage at:

    1. -20°C to -70°C for 12 months in lyophilized state;
    2. -70°C for 3 months under sterile conditions after reconstitution.
  • Background
    The protein encoded by this gene is a component of the vitamin A visual cycle of the retina which supplies the 11-cis retinal chromophore of the photoreceptors opsin visual pigments. It is a member of the carotenoid cleavage oxygenase superfamily. All members of this superfamily are non-heme iron oxygenases with a seven-bladed propeller fold and oxidatively cleave carotenoid carbon:carbon double bonds. However, the protein encoded by this gene has acquired a divergent function that involves the concerted O-alkyl ester cleavage of its all-trans retinyl ester substrate and all-trans to 11-cis double bond isomerization of the retinyl moiety. As such, it performs the essential enzymatic isomerization step in the synthesis of 11-cis retinal. Mutations in this gene are associated with early-onset severe blinding disorders such as Leber congenital.
  • Clinical and Translational Updates

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価格(JPY) : 112,000

価格(JPY) : 784,000

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  • Number of Drugs in Clinical Trials:4 Details
  • Latest Research Phase:Approved

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