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Six5 antibody (Middle Region)

The Rabbit Polyclonal anti-Six5 antibody has been validated for WB, IHC (p) and EIA. It is suitable to detect Six5 in samples from Human.
Catalog No. ABIN954812

Quick Overview for Six5 antibody (Middle Region) (ABIN954812)

Target

See all Six5 (SIX5) Antibodies
Six5 (SIX5) (Homeobox protein SIX5 (SIX5))

Reactivity

  • 22
  • 12
  • 1
Human

Host

  • 23
Rabbit

Clonality

  • 23
Polyclonal

Conjugate

  • 11
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This Six5 antibody is un-conjugated

Application

  • 16
  • 13
  • 8
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Enzyme Immunoassay (EIA)
  • Binding Specificity

    • 7
    • 4
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 264-294, Middle Region

    Specificity

    This antibody recognizes Human SIX5 (Center).

    Purification

    Protein A column, followed by peptide affinity purification

    Immunogen

    KLH conjugated synthetic peptide between 264-294 amino acids from the Central region of Human SIX5. Genename: SIX5

    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

    Six5 (SIX5) (Homeobox protein SIX5 (SIX5))

    Alternative Name

    SIX5

    Background

    The protein encoded by this gene is a homeodomain-containing transcription factor that appears to function in the regulation of organogenesis. This gene is located downstream of the dystrophia myotonica-protein kinase gene. Mutations in this gene are a cause of branchiootorenal syndrome type 2.Synonyms: DM locus-associated homeodomain protein, DMAHP, Homeobox protein SIX5, Sine oculis homeobox homolog 5

    Molecular Weight

    74562 Da

    Gene ID

    147912

    NCBI Accession

    NP_787071
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