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GTF2I antibody (C-Term)

This Rabbit Polyclonal antibody specifically detects GTF2I in WB, IF, IHC (p) and FACS. It exhibits reactivity toward Human.
Catalog No. ABIN390868

Quick Overview for GTF2I antibody (C-Term) (ABIN390868)

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

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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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  • 7
  • 5
  • 2
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  • 2
  • 2
  • 1
Western Blotting (WB), Immunofluorescence (IF), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Flow Cytometry (FACS)

Clone

RB20983
  • Binding Specificity

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    • 1
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    AA 956-985, C-Term

    Predicted Reactivity

    Rat

    Purification

    This antibody is purified through a protein A column, followed by peptide affinity purification.

    Immunogen

    This GTF2I antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 956-985 amino acids from the C-terminal region of human GTF2I.

    Isotype

    Ig Fraction
  • Application Notes

    IF: 1:25. IF: 1:10~50. WB: 1:1000. IHC-P: 1:50~100. FC: 1:10~50

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) 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,-20 °C

    Storage Comment

    Maintain refrigerated at 2-8 °C for up to 6 months. For long term storage store at -20 °C in small aliquots to prevent freeze-thaw cycles.

    Expiry Date

    6 months
  • Target

    GTF2I (General Transcription Factor III (GTF2I))

    Alternative Name

    GTF2I

    Background

    GTF2I is a multifunctional phosphoprotein with roles in transcription and signal transduction. It is deleted in Williams-Beuren syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at chromosome 7q11.23.

    Molecular Weight

    112416

    Gene ID

    2969

    NCBI Accession

    NP_001157108, NP_001267729, NP_001509, NP_127492, NP_127493, NP_127494

    UniProt

    P78347
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