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Adaptor-Related Protein Complex 3, mu 1 Subunit (AP3M1) (C-Term) Peptide

AP3M1 Reactivité: Humain Hôte: Synthetic BP, WB
N° du produit ABIN5512843
  • Antigène Tous les produits AP3M1
    AP3M1 (Adaptor-Related Protein Complex 3, mu 1 Subunit (AP3M1))
    Protein Region
    C-Term
    Origine
    Humain
    Source
    Synthetic
    Application
    Blocking Peptide (BP), Western Blotting (WB)
    Séquence
    TQGSYTFDPV TKVLTWDVGK ITPQKLPSLK GLVNLQSGAP KPEENPSLNI
    Attributs du produit
    This is a synthetic peptide designed for use in combination with anti-AP3M1 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
    AP3M1 (Adaptor-Related Protein Complex 3, mu 1 Subunit (AP3M1))
    Synonymes
    1200013D09Rik Peptide, C78982 Peptide, R75378 Peptide, P47a Peptide, adaptor related protein complex 3 mu 1 subunit Peptide, adaptor-related protein complex 3, mu 1 subunit Peptide, AP3M1 Peptide, Ap3m1 Peptide
    Sujet
    The protein encoded by this gene is the medium subunit of AP-3, which is an adaptor-related protein complex associated with the Golgi region as well as more peripheral intracellular structures. AP-3 facilitates the budding of vesicles from the Golgi membrane, and it may directly function in protein sorting to the endosomal/lysosomal system. AP-3 is a heterotetrameric protein complex composed of two large subunits (delta and beta3), a medium subunit (mu3), and a small subunit (sigma 3). Mutations in one of the large subunits of AP-3 have been associated with the Hermansky-Pudlak syndrome, a genetic disorder characterized by defective lysosome-related organelles. Alternative splicing of this gene results in multiple transcript variants.

    Protein Size: 418
    ID gène
    26985
    NCBI Accession
    NM_012095, NP_036227
    UniProt
    Q9Y2T2
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