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BBS5 anticorps (AA 224-317) (FITC)

BBS5 Reactivité: Humain Hôte: Lapin Polyclonal FITC
N° du produit ABIN7145244
  • Antigène Voir toutes BBS5 Anticorps
    BBS5 (Bardet-Biedl Syndrome 5 (BBS5))
    Épitope
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    AA 224-317
    Reactivité
    • 15
    • 7
    • 7
    • 4
    • 4
    • 3
    • 3
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    Humain
    Hôte
    • 12
    • 3
    Lapin
    Clonalité
    • 14
    • 1
    Polyclonal
    Conjugué
    • 13
    • 1
    • 1
    Cet anticorp BBS5 est conjugé à/à la FITC
    Application
    Veuillez nous consulter SVP
     Réactivité croisée
    Humain
    Purification
    >95%, Protein G purified
    Immunogène
    Recombinant Human Bardet-Biedl syndrome 5 protein (224-317AA)
    Isotype
    IgG
    Top Product
    Discover our top product BBS5 Anticorps primaire
  • Restrictions
    For Research Use only
  • Format
    Liquid
    Buffer
    Preservative: 0.03 % Proclin 300
    Constituents: 50 % Glycerol, 0.01M PBS, pH 7.4
    Agent conservateur
    ProClin
    Précaution d'utilisation
    This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Stock
    -20 °C,-80 °C
    Stockage commentaire
    Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
  • Antigène
    BBS5 (Bardet-Biedl Syndrome 5 (BBS5))
    Autre désignation
    BBS5 (BBS5 Produits)
    Synonymes
    anticorps zgc:56578, anticorps 1700049I01Rik, anticorps 2700023J09Rik, anticorps Bardet-Biedl syndrome 5, anticorps Bardet-Biedl syndrome 5 (human), anticorps bbs5, anticorps BBS5, anticorps Bbs5
    Sujet

    Background: The BBSome complex is thought to function as a coat complex required for sorting of specific membrane proteins to the primary cilia. The BBSome complex is required for ciliogenesis but is dispensable for centriolar satellite function. This ciliogenic function is mediated in part by the Rab8 GDP/GTP exchange factor, which localizes to the basal body and contacts the BBSome. Rab8(GTP) enters the primary cilium and promotes extension of the ciliary membrane. Firstly the BBSome associates with the ciliary membrane and binds to RAB3IP/Rabin8, the guanosyl exchange factor (GEF) for Rab8 and then the Rab8-GTP localizes to the cilium and promotes docking and fusion of carrier vesicles to the base of the ciliary membrane. The BBSome complex, together with the LTZL1, controls SMO ciliary trafficking and contributes to the sonic hedgehog (SHH) pathway regulation. Required for BBSome complex ciliary localization but not for the proper complex assembly.

    Aliases: Bardet Biedl syndrome 5 protein antibody, Bardet-Biedl syndrome 5 protein antibody, BBS5 antibody, BBS5_HUMAN antibody

    UniProt
    Q8N3I7
    Pathways
    Signalisation Hedgehog
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