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PPOX antibody (N-Term)

This Rabbit Polyclonal antibody specifically detects PPOX in WB. It exhibits reactivity toward Human, Mouse and Rat.
Catalog No. ABIN633874

Quick Overview for PPOX antibody (N-Term) (ABIN633874)

Target

See all PPOX Antibodies
PPOX (Protoporphyrinogen Oxidase (PPOX))

Reactivity

  • 40
  • 23
  • 19
  • 4
  • 4
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
Human, Mouse, Rat

Host

  • 40
  • 7
Rabbit

Clonality

  • 41
  • 6
Polyclonal

Conjugate

  • 28
  • 4
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
This PPOX antibody is un-conjugated

Application

  • 28
  • 18
  • 13
  • 10
  • 9
  • 4
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB)
  • Binding Specificity

    • 6
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    N-Term

    Specificity

    PPOX antibody was raised against the N terminal of PPOX

    Purification

    Affinity purified

    Immunogen

    PPOX antibody was raised using the N terminal of PPOX corresponding to a region with amino acids SSERLGGWIRSVRGPNGAIFELGPRGIRPAGALGARTLLLVSELGLDSEV
  • Application Notes

    WB: 1 µg/mL
    Optimal conditions should be determined by the investigator.

    Comment

    PPOX Blocking Peptide, (ABIN5615504), is also available for use as a blocking control in assays to test for specificity of this PPOX antibody

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

    Lyophilized powder. Add distilled water for a 1 mg/mL concentration of PPOX antibody in PBS

    Concentration

    Lot specific

    Buffer

    PBS

    Handling Advice

    Avoid repeated freeze/thaw cycles.
    Dilute only prior to immediate use.

    Storage

    4 °C/-20 °C

    Storage Comment

    Store at 2-8 °C for short periods. For longer periods of storage, store at -20 °C.
  • Target

    PPOX (Protoporphyrinogen Oxidase (PPOX))

    Alternative Name

    PPOX

    Background

    This gene encodes the penultimate enzyme of heme biosynthesis, which catalyzes the 6-electron oxidation of protoporphyrinogen IX to form protoporphyrin IX. Mutations in this gene cause variegate porphyria, an autosomal dominant disorder of heme metabolism resulting from a deficiency in protoporphyrinogen oxidase, an enzyme located on the inner mitochondrial membrane. Alternatively spliced transcript variants encoding the same protein have been identified.

    Molecular Weight

    51 kDa (MW of target protein)

    Pathways

    Synaptic Membrane, Feeding Behaviour
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