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AMBN antibody (C-Term)

This Rabbit Polyclonal antibody specifically detects AMBN in WB. It exhibits reactivity toward Human.
Catalog No. ABIN1449916
$618.00
Plus shipping costs $50.00
100 μL
Shipping to: United States
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Quick Overview for AMBN antibody (C-Term) (ABIN1449916)

Target

See all AMBN Antibodies
AMBN (Ameloblastin (Enamel Matrix Protein) (AMBN))

Reactivity

  • 16
  • 3
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
Human

Host

  • 14
  • 2
Rabbit

Clonality

  • 16
Polyclonal

Conjugate

  • 12
  • 2
  • 1
  • 1
This AMBN antibody is un-conjugated

Application

  • 11
  • 8
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB)
  • Binding Specificity

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

    Sequence

    RPGFEGMPHN PAMGGDFTLE FDSPVAATKG PENEEGGAQG SPMPEANPDN

    Cross-Reactivity (Details)

    Species reactivity (tested):Human

    Purification

    Purified using peptide immunoaffinity column

    Immunogen

    Synthetic peptide directed towards the C terminal of human Ameloblastin
  • Application Notes

    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.

    Handling Advice

    Avoid repeated freezing and thawing.

    Storage

    4 °C/-20 °C

    Storage Comment

    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.
  • Target

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

    Alternative Name

    Ameloblastin

    Background

    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

    Gene ID

    258

    NCBI Accession

    NM_016519
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