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FOXN1 antibody (Middle Region)

The Rabbit Polyclonal anti-FOXN1 antibody has been validated for WB, FACS and EIA. It is suitable to detect FOXN1 in samples from Human.
Catalog No. ABIN952376

Quick Overview for FOXN1 antibody (Middle Region) (ABIN952376)

Target

See all FOXN1 Antibodies
FOXN1 (Forkhead Box N1 (FOXN1))

Reactivity

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Human

Host

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Rabbit

Clonality

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Polyclonal

Conjugate

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This FOXN1 antibody is un-conjugated

Application

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Western Blotting (WB), Flow Cytometry (FACS), Enzyme Immunoassay (EIA)
  • Binding Specificity

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    AA 357-386, Middle Region

    Specificity

    This antibody recognizes Human FOXN1 (Center).

    Purification

    Protein A column, followed by peptide affinity purification

    Immunogen

    KLH conjugated synthetic peptide between 357-386 amino acids from the Central region of human FOXN1

    Isotype

    Ig Fraction
  • Application Notes

    Optimal working dilution should be determined by the investigator.

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.25 mg/mL

    Buffer

    PBS containing 0.09 % (W/V) Sodium Azide as preservative

    Preservative

    Sodium azide

    Precaution of Use

    This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Handling Advice

    Avoid repeated freezing and thawing.

    Storage

    4 °C/-20 °C

    Storage Comment

    Store undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.
  • Target

    FOXN1 (Forkhead Box N1 (FOXN1))

    Alternative Name

    FOXN1

    Background

    Mutations in the winged-helix transcription factor gene at the nude locus in mice and rats produce the pleiotropic phenotype of hairlessness and athymia, resulting in a severely compromised immune system. This gene is orthologous to the mouse and rat genes and encodes a similar DNA-binding transcription factor that is thought to regulate keratin gene expression. A mutation in this gene has been correlated with T-cell immunodeficiency, the skin disorder congenital alopecia, and nail dystrophy. Alternative splicing in the 5' UTR of this gene has been observed. [provided by RefSeq].Synonyms: Forkhead box protein N1, RONU, WHN, Winged-helix transcription factor nude

    Molecular Weight

    68925 Da

    Gene ID

    8456

    NCBI Accession

    NP_003584
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