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Ceruloplasmin antibody (AA 20-258)

This Rabbit Polyclonal antibody specifically detects Ceruloplasmin in WB and IHC (p). It exhibits reactivity toward Rat and Mouse.
Catalog No. ABIN4950633
$625.62
Plus shipping costs $50.00
100 μg
Shipping to: United States
Delivery in 2 to 4 Business Days

Quick Overview for Ceruloplasmin antibody (AA 20-258) (ABIN4950633)

Target

See all Ceruloplasmin (CP) Antibodies
Ceruloplasmin (CP) (Ceruloplasmin (Ferroxidase) (CP))

Reactivity

  • 61
  • 11
  • 10
Rat, Mouse

Host

  • 54
  • 9
  • 6
  • 3
  • 1
Rabbit

Clonality

  • 62
  • 9
Polyclonal

Conjugate

  • 43
  • 11
  • 8
  • 5
  • 2
  • 2
  • 2
This Ceruloplasmin antibody is un-conjugated

Application

  • 44
  • 34
  • 31
  • 15
  • 15
  • 11
  • 8
  • 8
  • 7
  • 6
  • 4
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
  • Binding Specificity

    • 10
    • 7
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 20-258

    Purification

    Antigen affinity

    Immunogen

    Amino acids 20-258 of mouse Ceruloplasmin were used as the immunogen for the CP antibody.

    Isotype

    IgG
  • Application Notes

    Optimal dilution of the CP antibody should be determined by the researcher.\. Western blot: 0.1-0.5 μg/mL,IHC (Paraffin): 0.5-1 μg/mL

    Restrictions

    For Research Use only
  • Buffer

    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

    Storage

    -20 °C

    Storage Comment

    After reconstitution, the CP antibody can be stored for up to one month at 4°C. For long-term, aliquot and store at -20°C. Avoid repeated freezing and thawing.
  • Target

    Ceruloplasmin (CP) (Ceruloplasmin (Ferroxidase) (CP))

    Alternative Name

    Ceruloplasmin / CP

    Background

    Ceruloplasmin (or Caeruloplasmin) is a ferroxidase enzyme that in humans is encoded by the CP gene. It is mapped to 3q23-q25. The protein encoded by this gene is a metalloprotein that binds most of the copper in plasma and is involved in the peroxidation of Fe(II)transferrin to Fe(III) transferrin. Mutations in this gene cause aceruloplasminemia, which results in iron accumulation and tissue damage, and is associated with diabetes and neurologic abnormalities. Two transcript variants, one protein-coding and the other not protein-coding, have been found for this gene.

    UniProt

    Q61147

    Pathways

    Transition Metal Ion Homeostasis
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