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TDG anticorps (AA 1-410)

Cet anticorps anti-TDG est un anticorps Souris Monoclonal détectant TDG dans WB, ELISA, IF et ICC. Adapté pour Humain.
N° du produit ABIN5776190

Aperçu rapide pour TDG anticorps (AA 1-410) (ABIN5776190)

Antigène

Voir toutes TDG Anticorps
TDG (Thymine-DNA Glycosylase (TDG))

Reactivité

  • 51
  • 18
  • 10
  • 2
  • 2
Humain

Hôte

  • 39
  • 12
Souris

Clonalité

  • 42
  • 10
Monoclonal

Conjugué

  • 45
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp TDG est non-conjugé

Application

  • 41
  • 13
  • 11
  • 10
  • 6
  • 6
  • 5
  • 3
  • 2
  • 2
  • 1
Western Blotting (WB), ELISA, Immunofluorescence (IF), Immunocytochemistry (ICC)

Clone

AT2F7
  • Épitope

    • 5
    • 5
    • 4
    • 3
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 1-410

    Immunogène

    Recombinant human TDG (1-410aa) purified from E. coli

    Isotype

    IgG1 kappa
  • Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 mg/mL

    Stock

    4 °C,-20 °C,-80 °C

    Stockage commentaire

    Can be stored at +2°C to +8°C for 1 week. For long term storage, aliquot and store at -20°C to -80°C. Avoid repeated freezing and thawing cycles.
  • Antigène

    TDG (Thymine-DNA Glycosylase (TDG))

    Autre désignation

    TDG

    Sujet

    G/T mismatch-specific thymine DNA glycosylase is an enzyme that in humans is encoded by the TDG gene. Several bacterial proteins have strong sequence homology with this protein. The protein encoded by this gene belongs to the TDG/mug DNA glycosylase family. Thymine-DNA glycosylase (TDG) removes thymine moieties from G/T mismatches by hydrolyzing the carbon-nitrogen bond between the sugar-phosphate backbone of DNA and the mispaired thymine. With lower activity, this enzyme also removes thymine from C/T and T/T mispairings. TDG can also remove uracil and 5-bromouracil from mispairings with guanine. This enzyme plays a central role in cellular defense against genetic mutation caused by the spontaneous deamination of 5-methylcytosine and cytosine. This gene may have a pseudogene in the p arm of chromosome 12.

    Pathways

    Réparation de l'ADN, Chromatin Binding
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