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PPOX antibody (N-Term)

PPOX Reactivity: Human, Mouse, Rat WB Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN633874
  • Target See all PPOX Antibodies
    PPOX (Protoporphyrinogen Oxidase (PPOX))
    Binding Specificity
    • 5
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    N-Term
    Reactivity
    • 37
    • 23
    • 16
    • 4
    • 4
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    Human, Mouse, Rat
    Host
    • 35
    • 5
    Rabbit
    Clonality
    • 36
    • 4
    Polyclonal
    Conjugate
    • 21
    • 4
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    This PPOX antibody is un-conjugated
    Application
    • 21
    • 11
    • 9
    • 4
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    Western Blotting (WB)
    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
    Top Product
    Discover our top product PPOX Primary Antibody
  • Application Notes
    WB: 1 µg/mL
    Optimal conditions should be determined by the investigator.
    Comment

    PPOX Blocking Peptide, catalog no. 33R-8796, 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 (PPOX Products)
    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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