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FECH antibody

This Rabbit Polyclonal antibody specifically detects FECH in WB and ELISA. It exhibits reactivity toward Human, Mouse, Rat and Dog.
Catalog No. ABIN2462452

Quick Overview for FECH antibody (ABIN2462452)

Target

See all FECH Antibodies
FECH (Ferrochelatase (FECH))

Reactivity

  • 39
  • 27
  • 23
  • 3
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
Human, Mouse, Rat, Dog

Host

  • 35
  • 6
Rabbit

Clonality

  • 37
  • 4
Polyclonal

Conjugate

  • 21
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This FECH antibody is un-conjugated

Application

  • 34
  • 13
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  • 6
  • 6
  • 4
  • 3
  • 2
  • 1
Western Blotting (WB), ELISA
  • Purification

    Antibody is purified by protein A chromatography method.

    Immunogen

    Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human FECH.
  • Application Notes

    FECH antibody can be used for detection of FECH by ELISA at 1:1562500. FECH antibody can be used for detection of FECH by western blot at 2.5 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

    Add 50 ?L of distilled water. Final antibody concentration is 1 mg/mL.

    Concentration

    1 mg/mL

    Buffer

    Antibody is lyophilized in PBS buffer with 2 % sucrose.

    Handling Advice

    As with any antibody avoid repeat freeze-thaw cycles.

    Storage

    4 °C/-20 °C

    Storage Comment

    For short periods of storage (days) store at 4 °C. For longer periods of storage, store FECH antibody at -20 °C.
  • Target

    FECH (Ferrochelatase (FECH))

    Alternative Name

    FECH

    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, 48 kDa

    Gene ID

    2235

    NCBI Accession

    NP_001012533

    UniProt

    Q8NAN0

    Pathways

    Transition Metal Ion Homeostasis
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