Forkhead Box C1 (FOXC1) Peptide
FOXC1
Reactivity: Human
Host: Synthetic
BP, WB
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- Target See all FOXC1 products
- FOXC1 (Forkhead Box C1 (FOXC1))
- Origin
- Human
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Source
- Synthetic
- Application
- Blocking Peptide (BP), Western Blotting (WB)
- Characteristics
- This is a synthetic peptide designed for use in combination with anti-FOXC1 antibody (Catalog #: ARP32300_T100). 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
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- Application Notes
- Each Investigator should determine their own optimal working dilution for specific applications.
- Restrictions
- For Research Use only
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- 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.
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- Target
- FOXC1 (Forkhead Box C1 (FOXC1))
- Synonyms
- ARA Peptide, FKHL7 Peptide, FREAC-3 Peptide, FREAC3 Peptide, IGDA Peptide, IHG1 Peptide, IRID1 Peptide, RIEG3 Peptide, FoxC1 Peptide, fkhl7 Peptide, freac-3 Peptide, freac3 Peptide, igda Peptide, ihg1 Peptide, irid1 Peptide, rieg3 Peptide, xfd-11 Peptide, ara Peptide, FOXC1 Peptide, foxc1 Peptide, Fkh1 Peptide, Mf1 Peptide, Mf4 Peptide, ch Peptide, fkh-1 Peptide, frkhda Peptide, CFKH-1 Peptide, XFD-11 Peptide, foxc1.2 Peptide, id:ibd5079 Peptide, forkhead box C1 Peptide, forkhead box C1 S homeolog Peptide, forkhead box C1 L homeolog Peptide, Forkhead box protein C1 Peptide, winged helix transcription factor XFD-11 Peptide, forkhead box C1b Peptide, FOXC1 Peptide, Foxc1 Peptide, foxc1.S Peptide, foxc1 Peptide, foxc1.L Peptide, foxc1-A Peptide, foxc1b Peptide
- Background
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FOXC1 belongs to the forkhead family of transcription factors which is characterized by a distinct DNA-binding forkhead domain. The specific function of this gene has not yet been determined, however, it has been shown to play a role in the regulation of embryonic and ocular development. Mutations in this gene cause various glaucoma phenotypes including primary congenital glaucoma, autosomal dominant iridogoniodysgenesis anomaly, and Axenfeld-Rieger anomaly.
Alias Symbols: ARA, IGDA, IHG1, FKHL7, IRID1, RIEG3, FREAC3, FREAC-3
Protein Interaction Partner: HMGB1
Protein Size: 553 - Molecular Weight
- 57 kDa
- Gene ID
- 2296
- NCBI Accession
- NM_001453, NP_001444
- UniProt
- Q12948
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