Forkhead Box E1 (Thyroid Transcription Factor 2) (FOXE1) Peptide
FOXE1
Reactivity: Human
Host: Synthetic
BP, WB
Catalog No. ABIN977008
Quick Overview for Forkhead Box E1 (Thyroid Transcription Factor 2) (FOXE1) Peptide (ABIN977008)
Target
FOXE1
(Forkhead Box E1 (Thyroid Transcription Factor 2) (FOXE1))
Origin
Human
Source
Synthetic
Application
Blocking Peptide (BP), Western Blotting (WB)
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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.
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Purification
- Purified
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Application Notes
- 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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Handling Advice
- Avoid repeated freeze-thaw cycles.
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Storage
- -20 °C
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Storage Comment
- 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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Background
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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 -
Molecular Weight
- 38 kDa
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Gene ID
- 2304
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NCBI Accession
- NM_004473, NP_004464
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UniProt
- O00358
Target
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