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PPOX anticorps (N-Term)

Cet anticorps Lapin Polyclonal détecte spécifiquement PPOX dans WB. Il présente une réactivité envers Humain, Souris et Rat.
N° du produit ABIN633874

Aperçu rapide pour PPOX anticorps (N-Term) (ABIN633874)

Antigène

Voir toutes PPOX Anticorps
PPOX (Protoporphyrinogen Oxidase (PPOX))

Reactivité

  • 38
  • 23
  • 18
  • 4
  • 4
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
Humain, Souris, Rat

Hôte

  • 37
  • 7
Lapin

Clonalité

  • 38
  • 6
Polyclonal

Conjugué

  • 25
  • 4
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
Cet anticorp PPOX est non-conjugé

Application

  • 25
  • 15
  • 10
  • 9
  • 7
  • 3
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB)
  • Épitope

    • 5
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    N-Term

    Specificité

    PPOX antibody was raised against the N terminal of PPOX

    Purification

    Affinity purified

    Immunogène

    PPOX antibody was raised using the N terminal of PPOX corresponding to a region with amino acids SSERLGGWIRSVRGPNGAIFELGPRGIRPAGALGARTLLLVSELGLDSEV
  • Indications d'application

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

    Commentaires

    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

    Conseil sur la manipulation

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

    Stock

    4 °C/-20 °C

    Stockage commentaire

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

    PPOX (Protoporphyrinogen Oxidase (PPOX))

    Autre désignation

    PPOX

    Sujet

    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.

    Poids moléculaire

    51 kDa (MW of target protein)

    Pathways

    Synaptic Membrane, Feeding Behaviour
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