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Forkhead Box E1 (Thyroid Transcription Factor 2) (FOXE1) Peptide

FOXE1 Reactivity: Human Host: Synthetic BP, WB
Catalog No. ABIN977008
  • Target See all FOXE1 products
    FOXE1 (Forkhead Box E1 (Thyroid Transcription Factor 2) (FOXE1))
    Origin
    Human
    Source
    • 3
    Synthetic
    Application
    Blocking Peptide (BP), Western Blotting (WB)
    Characteristics
    This is a synthetic peptide designed for use in combination with anti-FOXE1 antibody (Catalog #: ARP31705_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
  • Application Notes
    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.
    Handling Advice
    Avoid repeated freeze-thaw cycles.
    Storage
    -20 °C
    Storage Comment
    For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
  • Target
    FOXE1 (Forkhead Box E1 (Thyroid Transcription Factor 2) (FOXE1))
    Synonyms
    FKHL15 Peptide, FOXE2 Peptide, HFKH4 Peptide, HFKL5 Peptide, TITF2 Peptide, TTF-2 Peptide, TTF2 Peptide, Titf2 Peptide, Ttf-2 Peptide, Ci-FoxE Peptide, Foxe1 Peptide, FoxE5 Peptide, ttf2 Peptide, foxe2 Peptide, hfkh4 Peptide, hfkl5 Peptide, titf2 Peptide, ttf-2 Peptide, fkhl15 Peptide, foxE1 Peptide, foxE Peptide, forkhead box E1 Peptide, foxE protein Peptide, forkhead box E1 L homeolog Peptide, FOXE1 Peptide, Foxe1 Peptide, foxE Peptide, foxe1.L Peptide, foxe1 Peptide, foxE1 Peptide
    Background
    FOXE1 belongs to the forkhead family of transcription factors, which is characterized by a distinct forkhead domain. It functions as a thyroid transcription factor which likely plays a crucial role in thyroid morphogenesis. Mutations in this gene are associated with congenital hypothyroidism and cleft palate with thyroid dysgenesis. The map localization of this gene suggests it may also be a candidate gene for squamous cell epithelioma and hereditary sensory neuropathy type I.This intronless gene belongs to the forkhead family of transcription factors, which is characterized by a distinct forkhead domain. This gene functions as a thyroid transcription factor which likely plays a crucial role in thyroid morphogenesis. Mutations in this gene are associated with congenital hypothyroidism and cleft palate with thyroid dysgenesis. The map localization of this gene suggests it may also be a candidate gene for squamous cell epithelioma and hereditary sensory neuropathy type I. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Entrez Gene record to access additional publications.

    Alias Symbols: FKHL15, FOXE2, HFKH4, HFKL5, TITF2, TTF-2, TTF2

    Protein Interaction Partner: PLCB3

    Protein Size: 373
    Molecular Weight
    38 kDa
    Gene ID
    2304
    NCBI Accession
    NM_004473, NP_004464
    UniProt
    O00358
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