Ferrochelatase (FECH) (Middle Region) Peptide
FECH
Reactivity: Human
Host: Synthetic
BP, WB
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- Target See all FECH products
- FECH (Ferrochelatase (FECH))
- Protein Region
- Middle Region
- 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-FECH antibody (Catalog #: ARP41683_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
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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
- FECH (Ferrochelatase (FECH))
- Synonyms
- AI894116 Peptide, Fcl Peptide, fch Peptide, zgc:109851 Peptide, EPP Peptide, FCE Peptide, CG2098 Peptide, Dmel\\CG2098 Peptide, GB15952 Peptide, ferrochelatase L homeolog Peptide, ferrochelatase Peptide, Ferrochelatase Peptide, ferrochelatase, mitochondrial Peptide, ferrochelatase HemH Peptide, ferrochelatase (predicted) Peptide, fech.L Peptide, hemH Peptide, Fech Peptide, FECH Peptide, fech Peptide, FeCH Peptide, LOC409922 Peptide, hem15 Peptide, APH_RS01140 Peptide
- Background
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FECH is localized to the mitochondrion, where it catalyzes the insertion of the ferrous form of iron into protoporphyrin IX in the heme synthesis pathway. Mutations in this gene are associated with erythropoietic protoporphyria. Two transcript variants encoding different isoforms have been found for this gene.The protein encoded by this gene is localized to the mitochondrion, where it catalyzes the insertion of the ferrous form of iron into protoporphyrin IX in the heme synthesis pathway. Mutations in this gene are associated with erythropoietic protoporphyria. Two transcript variants encoding different isoforms have been found for this gene.
Alias Symbols: EPP, FCE
Protein Interaction Partner: ABCB7,FECH,ABCB7,FECH,USP20,USP42
Protein Size: 423 - Molecular Weight
- 42 kDa
- Gene ID
- 2235
- NCBI Accession
- NM_000140, NP_000131
- UniProt
- P22830
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