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ZIC3 antibody (AA 113-455)

The Rabbit Polyclonal anti-ZIC3 antibody (ABIN7870153) specifically detects ZIC3 in WB, ELISA and FACS. The antibody is reactive with Human, Mouse and Rat samples.
Catalog No. ABIN7870153
$625.62
Plus shipping costs $50.00
100 μg
Shipping to: United States
Delivery in 2 to 4 Business Days

Quick Overview for ZIC3 antibody (AA 113-455) (ABIN7870153)

Target

See all ZIC3 Antibodies
ZIC3 (Zic Family Member 3 (ZIC3))

Reactivity

  • 30
  • 12
  • 5
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
Human, Mouse, Rat

Host

  • 23
  • 5
  • 2
Rabbit

Clonality

  • 25
  • 5
Polyclonal

Conjugate

  • 23
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This ZIC3 antibody is un-conjugated

Application

  • 19
  • 9
  • 8
  • 5
  • 4
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB), ELISA, Flow Cytometry (FACS)
  • Binding Specificity

    • 4
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 113-455

    Purpose

    ZIC3 Antibody

    Purification

    Antigen affinity purified

    Immunogen

    Recombinant human protein (amino acids N113-N455) was used as the immunogen for the ZIC3 antibody.

    Isotype

    IgG
  • Application Notes

    Optimal dilution of the ZIC3 antibody should be determined by the researcher.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Buffer

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

    Storage

    4 °C,-20 °C

    Storage Comment

    After reconstitution, the ZIC3 antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
  • Target

    ZIC3 (Zic Family Member 3 (ZIC3))

    Alternative Name

    ZIC3

    Background

    ZIC3 is a member of the Zinc finger of the cerebellum (ZIC) protein family. This gene encodes a member of the ZIC family of C2H2-type zinc finger proteins. This nuclear protein probably functions as a transcription factor in early stages of left-right body axis formation. Mutations in this gene cause X-linked visceral heterotaxy, which includes congenital heart disease and left-right axis defects in organs.

    UniProt

    O60481
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