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AMBN anticorps (C-Term)

Cet anticorps Lapin Polyclonal détecte spécifiquement AMBN dans WB. Il présente une réactivité envers Humain.
N° du produit ABIN1449916

Aperçu rapide pour AMBN anticorps (C-Term) (ABIN1449916)

Antigène

Voir toutes AMBN Anticorps
AMBN (Ameloblastin (Enamel Matrix Protein) (AMBN))

Reactivité

  • 14
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
Humain

Hôte

  • 12
  • 2
Lapin

Clonalité

  • 14
Polyclonal

Conjugué

  • 10
  • 2
  • 1
  • 1
Cet anticorp AMBN est non-conjugé

Application

  • 9
  • 7
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB)
  • Épitope

    • 6
    • 2
    • 2
    • 1
    • 1
    • 1
    C-Term

    Séquence

    RPGFEGMPHN PAMGGDFTLE FDSPVAATKG PENEEGGAQG SPMPEANPDN

    Réactivité croisée (Details)

    Species reactivity (tested):Human

    Purification

    Purified using peptide immunoaffinity column

    Immunogène

    Synthetic peptide directed towards the C terminal of human Ameloblastin
  • Indications d'application

    Optimal working dilution should be determined by the investigator.

    Restrictions

    For Research Use only
  • Reconstitution

    Add 50 μL of distilled water to a final concentration of 1 mg/mL.

    Conseil sur la manipulation

    Avoid repeated freezing and thawing.

    Stock

    4 °C/-20 °C

    Stockage commentaire

    Store lyophilized at 2-8 °C or at -20 °C long term. After reconstitution store the antibody undiluted at 2-8 °C for up to one month or in aliquots at -20 °C long term.
  • Antigène

    AMBN (Ameloblastin (Enamel Matrix Protein) (AMBN))

    Autre désignation

    Ameloblastin

    Sujet

    Ameloblastin is thought to represent an unique ameloblast-specific gene product that may be important in enamel matrix formation and mineralization. The gene is located on chromosome 4 near other genes associated with mineralized tissues: osteopontin, bone sialoprotein, and bone morphogenetic protein 3. Based on its cytogenetic location, this gene is a candidate gene for one form of the disorder, dentinogenesis imperfecta, and/or the disorder, autosomal dominant amylogenesis imperfecta.Synonyms: AMBN

    ID gène

    258

    NCBI Accession

    NM_016519
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