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TBC1D22A anticorps

TBC1D22A Reactivité: Humain ELISA, IHC Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN7131302
  • Antigène Voir toutes TBC1D22A Anticorps
    TBC1D22A (TBC1 Domain Family, Member 22A (TBC1D22A))
    Reactivité
    • 34
    • 5
    • 5
    • 4
    • 3
    • 3
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    Humain
    Hôte
    • 34
    Lapin
    Clonalité
    • 34
    Polyclonal
    Conjugué
    • 14
    • 4
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp TBC1D22A est non-conjugé
    Application
    • 24
    • 18
    • 14
    • 3
    • 1
    • 1
    ELISA, Immunohistochemistry (IHC)
     Réactivité croisée
    Humain, Souris
    Purification
    Antigen affinity purification
    Immunogène
    Fusion protein of Human TBC1D22A
    Isotype
    IgG
    Top Product
    Discover our top product TBC1D22A Anticorps primaire
  • Indications d'application
    ELISA:1:2000-1:5000, IHC:1:25-1:100,
    Restrictions
    For Research Use only
  • Format
    Liquid
    Buffer
    -20 °C, pH 7.4 PBS, 0.05 % Sodium azide, 40 % Glycerol
    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,-80 °C
    Stockage commentaire
    Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
  • Antigène
    TBC1D22A (TBC1 Domain Family, Member 22A (TBC1D22A))
    Autre désignation
    TBC1D22A (TBC1D22A Produits)
    Synonymes
    anticorps C22orf4, anticorps HSC79E021, anticorps BC023106, anticorps D15Ertd781e, anticorps RGD1306588, anticorps TBC1 domain family member 22A, anticorps TBC1 domain family, member 22a, anticorps TBC1D22A, anticorps Tbc1d22a
    Sujet

    Background: TBC1D22A (TBC1 domain family, member 22A), also known as C22orf4, is a 517 amino acid protein that contains one Rab-GAP TBC domain and is thought to function as a GTPase-activating protein for Rab family members. Multiple isoforms of TBC1D22A exist due to alternative splicing events. The gene encoding TBC1D22A maps to human chromosome 22, which houses over 500 genes and is the second smallest human chromosome. Mutations in several of the genes that map to chromosome 22 are involved in the development of Phelan-McDermid syndrome, neurofibromatosis type 2, autism and schizophrenia. Additionally, translocations between chromosomes 9 and 22 may lead to the formation of the Philadelphia chromosome and the subsequent production of the novel fusion protein BCR-Abl, a potent cell proliferation activator found in several types of leukemias.

    Aliases: TBC1D22A antibody, C22orf4 antibody, TBC1 domain family member 22A antibody

    UniProt
    Q8WUA7
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