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TDG antibody (AA 1-410)

This anti-TDG antibody is a Mouse Monoclonal antibody detecting TDG in WB, ELISA, IF and ICC. Suitable for Human.
Catalog No. ABIN5776190

Quick Overview for TDG antibody (AA 1-410) (ABIN5776190)

Target

See all TDG Antibodies
TDG (Thymine-DNA Glycosylase (TDG))

Reactivity

  • 52
  • 19
  • 11
  • 2
  • 2
Human

Host

  • 40
  • 12
Mouse

Clonality

  • 43
  • 10
Monoclonal

Conjugate

  • 46
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This TDG antibody is un-conjugated

Application

  • 42
  • 14
  • 11
  • 11
  • 6
  • 6
  • 5
  • 3
  • 3
  • 2
  • 1
Western Blotting (WB), ELISA, Immunofluorescence (IF), Immunocytochemistry (ICC)

Clone

AT2F7
  • Binding Specificity

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

    Immunogen

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

    Isotype

    IgG1 kappa
  • Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 mg/mL

    Storage

    4 °C,-20 °C,-80 °C

    Storage Comment

    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.
  • Target

    TDG (Thymine-DNA Glycosylase (TDG))

    Alternative Name

    TDG

    Background

    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

    DNA Damage Repair, Chromatin Binding
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