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GTF2I antibody (C-Term)

The Rabbit Polyclonal anti-GTF2I antibody has been validated for WB and IHC. It is suitable to detect GTF2I in samples from Human.
Catalog No. ABIN7449365

Quick Overview for GTF2I antibody (C-Term) (ABIN7449365)

Target

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

Reactivity

  • 52
  • 25
  • 19
  • 5
  • 4
  • 3
  • 3
  • 2
  • 2
  • 2
  • 1
  • 1
Human

Host

  • 48
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Rabbit

Clonality

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Polyclonal

Conjugate

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

Application

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  • 15
  • 15
  • 8
  • 5
  • 3
  • 2
  • 2
  • 2
  • 1
Western Blotting (WB), Immunohistochemistry (IHC)
  • Binding Specificity

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    • 3
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    • 1
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    C-Term

    Purpose

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

    Predicted Reactivity

    Rat

    Purification

    Affinity Purified

    Immunogen

    between AA 950 and C-term

    Isotype

    IgG
  • Application Notes

    IHC: 1:1,000 - 1:5,000. Epitope retrieval with citrate buffer pH 6.0 is recommended for FFPE tissue sections.

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

    Restrictions

    For Research Use only
  • Concentration

    1000 μg/mL

    Buffer

    Tris-citrate/phosphate buffer, pH 7 to 8 containing 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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