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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
$846.00
Plus shipping costs $50.00
0.4 mL
Shipping to: United States
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Quick Overview for FOXN1 antibody (Middle Region) (ABIN952376)

Target

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

Reactivity

  • 45
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  • 2
  • 2
  • 1
  • 1
  • 1
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Human

Host

  • 44
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Rabbit

Clonality

  • 45
Polyclonal

Conjugate

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  • 1
  • 1
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  • 1
  • 1
  • 1
  • 1
  • 1
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  • 1
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  • 1
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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