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GTF2I antibody (AA 985-998)

The Rabbit Polyclonal anti-GTF2I antibody has been validated for WB, IP and IHC (fp). It is suitable to detect GTF2I in samples from Human and Mouse.
Catalog No. ABIN7454740

Quick Overview for GTF2I antibody (AA 985-998) (ABIN7454740)

Target

See all GTF2I Antibodies
GTF2I (General Transcription Factor III (GTF2I))

Reactivity

  • 52
  • 24
  • 19
  • 5
  • 4
  • 3
  • 3
  • 2
  • 2
  • 2
  • 1
  • 1
Human, Mouse

Host

  • 48
  • 4
Rabbit

Clonality

  • 48
  • 4
Polyclonal

Conjugate

  • 35
  • 3
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This GTF2I antibody is un-conjugated

Application

  • 40
  • 23
  • 16
  • 15
  • 8
  • 4
  • 3
  • 2
  • 2
  • 1
  • 1
Western Blotting (WB), Immunoprecipitation (IP), Immunohistochemistry (Formalin-fixed Paraffin-embedded Sections) (IHC (fp))
  • Binding Specificity

    • 8
    • 8
    • 8
    • 4
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 985-998

    Purpose

    Rabbit anti-GTF2I/TFII-I Antibody, Affinity Purified

    Predicted Reactivity

    Rat,Bovine

    Purification

    Affinity Purified

    Immunogen

    between AA 985 and 998

    Isotype

    IgG
  • Application Notes

    IHC: 1:200 - 1:1,000. Epitope retrieval with citrate buffer pH 6.0 is recommended for FFPE tissue sections.

    IP: 2 - 5 μg/mg lysate

    WB: 1:2,000 - 1:10,000

    Restrictions

    For Research Use only
  • Concentration

    200 μg/mL

    Buffer

    Tris-buffered Saline containing 0.1 % BSA and 0.09 % Sodium Azide

    Preservative

    Sodium azide

    Precaution of Use

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Storage

    4 °C

    Expiry Date

    12 months
  • Target

    GTF2I (General Transcription Factor III (GTF2I))

    Alternative Name

    GTF2I/TFII-I

    Background

    Background: GTF2I/TFII-I is a multi-functional transcription factor that interacts with the basal transcription machinery and links upstream cellular signals to responsive activator complexes that associate with the C-FOS promoter and other response elements. Haploinsufficiency of GTF2I/TFII-I results in Williams-Beuren syndrome (WBS), a rare developmental disorder characterized by musculo-skeletal and cardiac abnormalities.

    Gene ID

    2969

    NCBI Accession

    NP_127492

    UniProt

    P78347
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