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GTF2I anticorps (N-Term)

Cet anticorps Lapin Polyclonal détecte spécifiquement GTF2I dans WB et IF. Il présente une réactivité envers Humain.
N° du produit ABIN1539271

Aperçu rapide pour GTF2I anticorps (N-Term) (ABIN1539271)

Antigène

Voir toutes GTF2I Anticorps
GTF2I (General Transcription Factor III (GTF2I))

Reactivité

  • 54
  • 27
  • 21
  • 6
  • 4
  • 3
  • 3
  • 2
  • 2
  • 2
  • 1
  • 1
Humain

Hôte

  • 49
  • 5
Lapin

Clonalité

  • 49
  • 5
Polyclonal

Conjugué

  • 37
  • 3
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp GTF2I est non-conjugé

Application

  • 42
  • 23
  • 16
  • 16
  • 8
  • 5
  • 3
  • 2
  • 2
  • 2
  • 1
Western Blotting (WB), Immunofluorescence (IF)

Clone

RB20972
  • Épitope

    • 8
    • 8
    • 7
    • 4
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 281-310, N-Term

    Homologie

    M, Rat

    Purification

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

    Immunogène

    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
  • Indications d'application

    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.

    Agent conservateur

    Sodium azide

    Précaution d'utilisation

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

    Stock

    4 °C,-20 °C

    Stockage commentaire

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

    Date de péremption

    6 months
  • Antigène

    GTF2I (General Transcription Factor III (GTF2I))

    Autre désignation

    GTF2I

    Sujet

    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.

    Poids moléculaire

    112416

    ID gène

    2969

    NCBI Accession

    NP_001157108, NP_001267729, NP_001509, NP_127492, NP_127493, NP_127494

    UniProt

    P78347
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