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OVOL2 antibody (AA 1-271)

This Rabbit Polyclonal antibody specifically detects OVOL2 in WB, ELISA, IF and FACS. It exhibits reactivity toward Human.
Catalog No. ABIN7869023
$625.62
Plus shipping costs $50.00
100 μg
Shipping to: United States
Delivery in 2 to 4 Business Days

Quick Overview for OVOL2 antibody (AA 1-271) (ABIN7869023)

Target

See all OVOL2 Antibodies
OVOL2 (Ovo-Like 2 (OVOL2))

Reactivity

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  • 2
  • 1
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  • 1
Human

Host

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Rabbit

Clonality

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Polyclonal

Conjugate

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  • 1
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  • 1
  • 1
  • 1
  • 1
  • 1
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  • 1
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This OVOL2 antibody is un-conjugated

Application

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Western Blotting (WB), ELISA, Immunofluorescence (IF), Flow Cytometry (FACS)
  • Binding Specificity

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    AA 1-271

    Purpose

    OVOL2 Antibody / Ovo-like 2

    Purification

    Antigen affinity purified

    Immunogen

    E. coli-derived recombinant human protein (amino acids M1-E271) was used as the immunogen for the OVOL2 antibody.

    Isotype

    IgG
  • Application Notes

    Optimal dilution of the OVOL2 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 OVOL2 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

    OVOL2 (Ovo-Like 2 (OVOL2))

    Alternative Name

    OVOL2

    Background

    This gene encodes a member of the evolutionarily conserved ovo-like protein family. Mammalian members of this family contain a single zinc finger domain composed of a tetrad of C2H2 zinc fingers with variable N- and C-terminal extensions that contain intrinsically disordered domains. Members of this family are involved in epithelial development and differentiation. Knockout of this gene in mouse results in early embryonic lethality with phenotypes that include neurectoderm expansion, impaired vascularization, and heart anomalies. In humans, allelic variants of this gene have been associated with posterior polymorphous corneal dystrophy.

    UniProt

    Q9BRP0

    Pathways

    Tube Formation
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