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TBC1D7 anticorps

TBC1D7 Reactivité: Humain, Souris, Rat WB Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN7075849
  • Antigène Voir toutes TBC1D7 Anticorps
    TBC1D7 (TBC1 Domain Family, Member 7 (TBC1D7))
    Reactivité
    • 25
    • 11
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    Humain, Souris, Rat
    Hôte
    • 23
    • 2
    Lapin
    Clonalité
    • 25
    Polyclonal
    Conjugué
    • 11
    • 4
    • 3
    • 3
    • 2
    • 2
    Cet anticorp TBC1D7 est non-conjugé
    Application
    • 20
    • 16
    • 1
    • 1
    • 1
    Western Blotting (WB)
     Réactivité croisée
    Humain, Rat
    Purification
    Affinity purification
    Immunogène
    Recombinant protein corresponding to Mouse TBC1D7
    Top Product
    Discover our top product TBC1D7 Anticorps primaire
  • Indications d'application
    WB (H,M,R) 1: 500- 1: 1000
    Restrictions
    For Research Use only
  • Format
    Liquid
    Buffer
    PBS, pH 7.4, 0.02 % sodium azide
    Agent conservateur
    Sodium azide
    Précaution d'utilisation
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Stock
    -20 °C
  • Antigène
    TBC1D7 (TBC1 Domain Family, Member 7 (TBC1D7))
    Autre désignation
    TBC1D7 (TBC1D7 Produits)
    Synonymes
    anticorps PIG51, anticorps TBC7, anticorps dJ257A7.3, anticorps 2610009C09Rik, anticorps TBC1 domain family member 7, anticorps TBC1 domain family, member 7, anticorps TBC1D7, anticorps Tbc1d7
    Sujet
    TBC1 domain family member 7 (TBC1D7, TBC7) belongs to a family of TBC (Tre-2/Bub2/Cdc16) containing proteins that function as GTPase-activating proteins (GAPs) . TBC1D7 was initially identified as a novel binding protein within the TSC1-TSC2 complex, where it was thought to associate with TSC1 . Additional research indicates that TBC1D7 is a third subunit of the TSC1-TSC2 complex that possesses Rheb-GAP activity and signals upstream of mTORC1. Knockdown of TBC1D7 limits the association between TSC1 and TSC2, resulting in reduced Rheb-GAP activity and increased mTORC1 signaling . Mutations in the corresponding TBC1D7 gene result in increased mTORC1 signaling, delayed autophagy, and are associated with intellectual disability (ID) and macrocrania.
    Poids moléculaire
    36 kDa
    ID gène
    67046
    NCBI Accession
    NP_001239568
    UniProt
    Q9D0K0
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