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Ferrochelatase (FECH) Peptide

FECH Reactivity: Mammalian Host: Synthetic BP, WB, IHC
Catalog No. ABIN940246
  • Target See all FECH products
    FECH (Ferrochelatase (FECH))
    Peptide Type
    Synthetic
    Origin
    Mammalian
    Source
    • 5
    Synthetic
    Application
    Blocking Peptide (BP), Western Blotting (WB), Immunohistochemistry (IHC)
    Sequence
    LDRDLMTLPI QNKLAPFIAK RRTPKIQEQY RRIGGGSPIK IWTSKQGEGM
    Characteristics
    A synthetic peptide for use as a blocking control in assays to test for specificity of FECH antibody,
    Alternative Names: FECH control peptide, FECH antibody Blocking Peptide, Anti-FECH Blocking Peptide, Ferrochelatase Blocking Peptide, Protoporphyria Blocking Peptide, EPP Blocking Peptide, FCE Blocking Peptide
  • Application Notes
    Optimal conditions should be determined by the investigator
    Restrictions
    For Research Use only
  • Format
    Lyophilized
    Reconstitution
    Add 100 µL of distilled water for a final peptide concentration is 1 mg/mL.
    Buffer
    PBS
    Handling Advice
    Avoid repeated freeze/thaw cycles.
    Storage
    -20 °C
    Storage Comment
    Store at -20 °C long term.
  • 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
    Ferrochelatase is localized to the mitochondrion where it catalyzes the insertion of the ferrous form of iron into protoporphyrin IX in the heme synthesis pathway. Defects in ferrochelatase are associated with protoporphyria.Ferrochelatase is localized to the mitochondrion where it catalyzes the insertion of the ferrous form of iron into protoporphyrin IX in the heme synthesis pathway. Defects in ferrochelatase are associated with protoporphyria. Two transcript variants encoding different isoforms have been found for this gene.
    Molecular Weight
    47 kDa
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