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TTC38 anticorps

TTC38 Reactivité: Humain, Souris ELISA, IHC, WB Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN7253539
  • Antigène Voir toutes TTC38 Anticorps
    TTC38 (Tetratricopeptide Repeat Domain 38 (TTC38))
    Reactivité
    Humain, Souris
    Hôte
    • 13
    • 1
    Lapin
    Clonalité
    • 14
    Polyclonal
    Conjugué
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp TTC38 est non-conjugé
    Application
    ELISA, Immunohistochemistry (IHC), Western Blotting (WB)
    Attributs du produit
    Polyclonal Antibody
    Purification
    Antigen affinity purification
    Immunogène
    Fusion protein of human TTC38
    Isotype
    IgG
    Top Product
    Discover our top product TTC38 Anticorps primaire
  • Indications d'application
    WB 1:1000-1:5000, IHC 1:50-1:300, ELISA 1:5000-1:10000
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    1.5 mg/mL
    Buffer
    PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4
    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
    Stockage commentaire
    Store at -20°C. Avoid freeze / thaw cycles.
  • Antigène
    TTC38 (Tetratricopeptide Repeat Domain 38 (TTC38))
    Autre désignation
    TTC38 (TTC38 Produits)
    Synonymes
    anticorps 9030019H09, anticorps fb96d09, anticorps si:ch211-249g22.2, anticorps wu:fb96d09, anticorps zgc:112407, anticorps tetratricopeptide repeat domain 38, anticorps tetratricopeptide repeat domain 38 S homeolog, anticorps TTC38, anticorps Ttc38, anticorps ttc38.S, anticorps ttc38
    Sujet
    TTC38 (tetratricopeptide repeat domain 38) is a 469 amino acid protein that contains three TPR repeats and belongs to the TTC38 family. The gene that encodes TTC38 consists of over 26,000 bases and maps to 22q13. Housing over 500 genes, chromosome 22 is the second smallest chromosome in the human genome. 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. In addition, 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.
    Poids moléculaire

    Observed_MW: Refer to figures

    Calculated_MW: 53 kDa

    UniProt
    Q5R3I4
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