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Visual System Homeobox 1 (VSX1) (Middle Region) Peptide

VSX1 Reactivity: Human Host: Synthetic BP, WB
Catalog No. ABIN986108
$160.46
Plus shipping costs $50.00
100 μg
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Quick Overview for Visual System Homeobox 1 (VSX1) (Middle Region) Peptide (ABIN986108)

Target

VSX1 (Visual System Homeobox 1 (VSX1))

Origin

Human

Source

  • 5
Synthetic

Application

Blocking Peptide (BP), Western Blotting (WB)
  • Protein Region

    Middle Region

    Characteristics

    This is a synthetic peptide designed for use in combination with anti-VSX1 antibody (Catalog #: ARP35882_P050). It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications.

    Purification

    Purified
  • Application Notes

    Each Investigator should determine their own optimal working dilution for specific applications.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

    Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.

    Concentration

    1 mg/mL

    Buffer

    Final peptide concentration is 1 mg/mL in PBS.

    Handling Advice

    Avoid repeated freeze-thaw cycles.

    Storage

    -20 °C

    Storage Comment

    For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
  • Target

    VSX1 (Visual System Homeobox 1 (VSX1))

    Background

    VSX1 contains a paired-like homeodomain and binds to the core of the locus control region of the red/green visual pigment gene cluster. VSX1 may regulate expression of the cone opsin genes early in development. Mutations in VSX1 can cause posterior polymorphous corneal dystrophy and keratoconus. Alternatively spliced transcript variants encoding different isoforms have been described.The protein encoded by this gene contains a paired-like homeodomain and binds to the core of the locus control region of the red/green visual pigment gene cluster. The encoded protein may regulate expression of the cone opsin genes early in development. Mutations in this gene can cause posterior polymorphous corneal dystrophy and keratoconus. Alternatively spliced transcript variants encoding different isoforms have been described.

    Alias Symbols: KTCN, PPCD, PPD, RINX, KTCN1, CAASDS

    Protein Size: 365

    Molecular Weight

    38 kDa

    Gene ID

    30813

    NCBI Accession

    NM_014588, NP_055403

    UniProt

    Q9NZR4
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