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MGMT anticorps

MGMT Reactivité: Rat, Souris IHC Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN7249814
  • Antigène Voir toutes MGMT Anticorps
    MGMT (O6-Methylguanine-DNA-Methyltransferase (MGMT))
    Reactivité
    • 73
    • 18
    • 5
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    Rat, Souris
    Hôte
    • 68
    • 11
    Lapin
    Clonalité
    • 61
    • 18
    Polyclonal
    Conjugué
    • 44
    • 6
    • 5
    • 5
    • 3
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    Cet anticorp MGMT est non-conjugé
    Application
    • 55
    • 33
    • 21
    • 19
    • 13
    • 13
    • 7
    • 7
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Immunohistochemistry (IHC)
    Attributs du produit
    Polyclonal Antibody
    Purification
    Affinity purification
    Immunogène
    Recombinant protein corresponding to Mouse MGMT
    Isotype
    IgG
    Top Product
    Discover our top product MGMT Anticorps primaire
  • Indications d'application
    IHC 1:100-1:500
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    260 μg/mL
    Buffer
    PBS with 0.02 % sodium azide, 1 % BSA and 50 % 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
    MGMT (O6-Methylguanine-DNA-Methyltransferase (MGMT))
    Autre désignation
    MGMT (MGMT Produits)
    Synonymes
    anticorps AGT, anticorps AI267024, anticorps Agat, anticorps O-6-methylguanine-DNA methyltransferase, anticorps MGMT, anticorps Mgmt
    Sujet
    MGMT (O6-methylguanine-DNA methyltransferase) is transcriptionally activated in response to DNA damage and functions to repair mutagenic and cytotoxic O6-alkylguanine lesions caused by carcinogens or cytostatic drugs. MGMT induction by ionising radiation does not occur in p53-deficient mice, suggesting that MGMT induction may require p53. Similarly, MGMT mRNA and protein were shown to be inducible by ionising radiation, only in cell lines that express functional p53, and not in cell lines that do not express wild type p53. In contrast, high MGMT activity was associated with the presence of mutant p53, in a study of oral cancer cell lines. Similarly, MGMT activity was significantly lower in ovarian tumors with wildtype p53 than in tumors with mutant p53, supporting the view that wildtype p53 down-regulates the basal MGMT promoter.
    UniProt
    P26187, P24528
    Pathways
    Réparation de l'ADN, Positive Regulation of Response to DNA Damage Stimulus
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