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Retinal Pigment Epithelium-Specific Protein 65kDa (RPE65) (Middle Region) Peptide

RPE65 Reactivité: Humain Hôte: Synthetic BP, WB
N° du produit ABIN5512452

Aperçu rapide pour Retinal Pigment Epithelium-Specific Protein 65kDa (RPE65) (Middle Region) Peptide (ABIN5512452)

Antigène

RPE65 (Retinal Pigment Epithelium-Specific Protein 65kDa (RPE65))

Origine

Humain

Source

  • 3
Synthetic

Application

Blocking Peptide (BP), Western Blotting (WB)
  • Protein Region

    Middle Region

    Séquence

    LFKFLSSWSL WGANYMDCFE SNETMGVWLH IADKKRKKYL NNKYRTSPFN

    Attributs du produit

    This is a synthetic peptide designed for use in combination with anti-RPE65 Antibody. It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications.
  • Indications d'application

    Optimal working dilution should be determined by the investigator.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

    Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.

    Stock

    -20 °C

    Stockage commentaire

    For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
  • Antigène

    RPE65 (Retinal Pigment Epithelium-Specific Protein 65kDa (RPE65))

    Sujet

    This gene encodes a protein which is located in the retinal pigment epithelium and is involved in the production of 11-cis retinal and in visual pigment regeneration. There are two forms of this protein, a soluble form called sRPE65, and a palmitoylated, membrane-bound form known as mRPE65. mRPE65 serves as the palmitoyl donor for lecithin retinol acyl transferase (LRAT), the enzyme that catalyzes the vitamin A to all trans retinol step of the chromophore regeneration process. Both mRPE65 and sRPE65 also serve as regulatory proteins, with the ratio and concentrations of these molecules playing a role in the inhibition of 11-cis retinal synthesis. Mutations in this gene have been associated with Leber congenital amaurosis type 2 (LCA2) and retinitis pigmentosa.

    Alias Symbols: RPE65,

    Protein Size: 533

    ID gène

    6121

    NCBI Accession

    NP_000320

    UniProt

    Q16518
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