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PPOX antibody

This Rabbit Polyclonal antibody specifically detects PPOX in WB. It exhibits reactivity toward Human.
Catalog No. ABIN2854549

Quick Overview for PPOX antibody (ABIN2854549)

Target

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

Reactivity

  • 40
  • 24
  • 20
  • 4
  • 4
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
Human

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)
  • Cross-Reactivity

    Human

    Characteristics

    Rabbit Polyclonal antibody to PPOX (protoporphyrinogen oxidase)
    PPOX antibody [N3C3]

    Purification

    Purified by antigen-affinity chromatography.

    Immunogen

    Recombinant protein encompassing a sequence within the center region of human PPOX. The exact sequence is proprietary.

    Isotype

    IgG
  • Application Notes

    WB: 1:500-1:3000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.

    Comment

    Positive Control: A549 , HCT116

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.82 mg/mL

    Buffer

    0.1M Tris-Glycine ( pH 7), 20 % Glycerol, 0.01 % Thimerosal

    Preservative

    Thimerosal (Merthiolate)

    Precaution of Use

    This product contains Thimerosal (Merthiolate): a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Storage

    4 °C,-20 °C

    Storage Comment

    Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.
  • Target

    PPOX (Protoporphyrinogen Oxidase (PPOX))

    Alternative Name

    protoporphyrinogen oxidase

    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.

    Cellular Localization: Mitochondrion inner membrane, Peripheral membrane protein, Intermembrane side

    Molecular Weight

    51 kDa

    Gene ID

    5498

    UniProt

    P50336

    Pathways

    Synaptic Membrane, Feeding Behaviour
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