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Forkhead Box P2 (FOXP2) Peptide

FOXP2 Reactivité: Humain Hôte: Synthetic BP, WB, IHC
N° du produit ABIN977077

Aperçu rapide pour Forkhead Box P2 (FOXP2) Peptide (ABIN977077)

Antigène

FOXP2 (Forkhead Box P2 (FOXP2))

Origine

Humain

Source

  • 6
Synthetic

Application

Blocking Peptide (BP), Western Blotting (WB), Immunohistochemistry (IHC)
  • Attributs du produit

    This is a synthetic peptide designed for use in combination with anti-FOXP2 antibody (Catalog #: ARP33750_P050). It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications.

    Purification

    Purified
  • Indications d'application

    Each Investigator should determine their own optimal working dilution for specific applications.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

    Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.

    Concentration

    1 mg/mL

    Buffer

    Final peptide concentration is 1 mg/mL in PBS.

    Conseil sur la manipulation

    Avoid repeated freeze-thaw cycles.

    Stock

    -20 °C

    Stockage commentaire

    For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
  • Antigène

    FOXP2 (Forkhead Box P2 (FOXP2))

    Sujet

    FOXP2 is an evolutionarily conserved transcription factor expressed in fetal and adult brain. This transcription factor is a member of the forkhead/winged-helix (FOX) family of transcription factors, and contains a FOX DNA-binding domain and a large polyglutamine tract. Members of the FOX family of transcription factors are regulators of embryogenesis. The product of this gene is thought to be required for proper development of speech and language regions of the brain during embryogenesis. Although a point mutation in this gene has been associated with the KE pedigree segregating developmental verbal dyspraxia, no association between mutations in this gene and another speech disorder, autism, has been found. Four alternative transcripts encoding three different isoforms have been identified.

    Alias Symbols: SPCH1, CAGH44, TNRC10

    Protein Interaction Partner: FOXP1,FOXP4,CTBP1,FOXP1,FOXP2,FOXP4,GATAD2B

    Protein Size: 715

    Poids moléculaire

    80 kDa

    ID gène

    93986

    NCBI Accession

    NM_014491, NP_055306
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