Forkhead Box E1 (Thyroid Transcription Factor 2) (FOXE1) Peptid
FOXE1
Reaktivität: Human
Wirt: Synthetic
BP, WB
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- Target Alle FOXE1 Produkte
- FOXE1 (Forkhead Box E1 (Thyroid Transcription Factor 2) (FOXE1))
- Spezies
- Human
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Quelle
- Synthetic
- Applikation
- Blocking Peptide (BP), Western Blotting (WB)
- Produktmerkmale
- 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.
- Aufreinigung
- Purified
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- Applikationshinweise
- Each Investigator should determine their own optimal working dilution for specific applications.
- Beschränkungen
- Nur für Forschungszwecke einsetzbar
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- Format
- Lyophilized
- Rekonstitution
- Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
- Konzentration
- 1 mg/mL
- Buffer
- Final peptide concentration is 1 mg/mL in PBS.
- Handhabung
- Avoid repeated freeze-thaw cycles.
- Lagerung
- -20 °C
- Informationen zur Lagerung
- For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
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- Target
- FOXE1 (Forkhead Box E1 (Thyroid Transcription Factor 2) (FOXE1))
- Synonyme
- 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
- Hintergrund
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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 - Molekulargewicht
- 38 kDa
- Gen-ID
- 2304
- NCBI Accession
- NM_004473, NP_004464
- UniProt
- O00358
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