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FECH antibody

The Rabbit Polyclonal anti-FECH antibody (ABIN7114185) specifically detects FECH in WB, IHC and ELISA. The antibody is reactive with Human, Mouse and Rat samples.
Catalog No. ABIN7114185
-15% Promotion 2026
$401.73
$472.62
save $70.89 (-15 %)
Plus shipping costs $50.00
100 μg
Shipping to: United States
Delivery in 13 to 16 Business Days

Quick Overview for FECH antibody (ABIN7114185)

Target

See all FECH Antibodies
FECH (Ferrochelatase (FECH))

Reactivity

  • 37
  • 27
  • 21
  • 4
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
Human, Mouse, Rat

Host

  • 33
  • 4
Rabbit

Clonality

  • 35
  • 2
Polyclonal

Conjugate

  • 17
  • 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

  • 30
  • 13
  • 7
  • 4
  • 3
  • 2
  • 2
  • 2
  • 1
Western Blotting (WB), Immunohistochemistry (IHC), ELISA
  • Purpose

    FECH antibody

    Purification

    Immunogen affinity purified

    Purity

    ≥95 % as determined by SDS-PAGE

    Immunogen

    ferrochelatase (protoporphyria)

    Isotype

    IgG
  • Application Notes

    WB: 1:500 - 1:2000, IHC: 1:50 - 1:100

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    PBS with 0.02 % sodium azide and 50 % glycerol pH 7.3,

    Preservative

    Sodium azide

    Precaution of Use

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Handling Advice

    Avoid repeated freeze / thaw cycles.

    Storage

    -20 °C

    Storage Comment

    -20°C for 12 months

    Expiry Date

    12 months
  • Target

    FECH (Ferrochelatase (FECH))

    Alternative Name

    FECH

    Background

    Synonyms: Ferrochelatase, mitochondrial|Heme synthase|Protoheme ferro-lyase|FECH

    Background: 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. A pseudogene of this gene is found on chromosome 3.

    Molecular Weight

    50 kDa

    Gene ID

    2235

    UniProt

    P22830

    Pathways

    Transition Metal Ion Homeostasis
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