Forkhead Box E1 (Thyroid Transcription Factor 2) (FOXE1) Peptide
FOXE1
Reactivité: Humain
Hôte: Synthetic
BP, WB
N° du produit ABIN977008
Aperçu rapide pour Forkhead Box E1 (Thyroid Transcription Factor 2) (FOXE1) Peptide (ABIN977008)
Antigène
FOXE1
(Forkhead Box E1 (Thyroid Transcription Factor 2) (FOXE1))
Origine
Humain
Source
Synthetic
Application
Blocking Peptide (BP), Western Blotting (WB)
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Attributs du produit
- 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.
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Purification
- Purified
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Indications d'application
- Each Investigator should determine their own optimal working dilution for specific applications.
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Restrictions
- For Research Use only
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Format
- Lyophilized
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Reconstitution
- Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
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Concentration
- 1 mg/mL
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Buffer
- Final peptide concentration is 1 mg/mL in PBS.
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Conseil sur la manipulation
- Avoid repeated freeze-thaw cycles.
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Stock
- -20 °C
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Stockage commentaire
- For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
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- FOXE1 (Forkhead Box E1 (Thyroid Transcription Factor 2) (FOXE1))
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Sujet
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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 -
Poids moléculaire
- 38 kDa
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ID gène
- 2304
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NCBI Accession
- NM_004473, NP_004464
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UniProt
- O00358
Antigène
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