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GTF2I antibody (N-Term)

This Rabbit Polyclonal antibody specifically detects GTF2I in WB and IF. It exhibits reactivity toward Human.
Catalog No. ABIN1539271

Quick Overview for GTF2I antibody (N-Term) (ABIN1539271)

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
  • 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
  • 14
  • 8
  • 5
  • 3
  • 2
  • 2
  • 2
  • 1
Western Blotting (WB), Immunofluorescence (IF)

Clone

RB20972
  • Binding Specificity

    • 8
    • 8
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    • 4
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
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    • 1
    • 1
    AA 281-310, N-Term

    Predicted Reactivity

    M, 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 281-310 amino acids from the N-terminal region of human GTF2I.

    Isotype

    Ig Fraction
  • Application Notes

    IF: 1:10~50. WB: 1:1000

    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

    GTF2I Antibody (N-term) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, keep at -20 °C.

    Expiry Date

    6 months
  • Target

    GTF2I (General Transcription Factor III (GTF2I))

    Alternative Name

    GTF2I

    Background

    This gene encodes 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. Alternative splicing results in multiple transcript variants. Related pseudogenes have been identified on chromosomes 7, 13 and 21.

    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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