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VSX1 antibody

VSX1 Reactivity: Human WB Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7264858
  • Target See all VSX1 Antibodies
    VSX1 (Visual System Homeobox 1 (VSX1))
    Reactivity
    • 31
    • 7
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    Human
    Host
    • 33
    Rabbit
    Clonality
    • 33
    Polyclonal
    Conjugate
    • 16
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This VSX1 antibody is un-conjugated
    Application
    • 26
    • 15
    • 1
    Western Blotting (WB)
    Characteristics
    Polyclonal Antibody
    Purification
    Affinity purification
    Immunogen
    Recombinant fusion protein of human VSX1 (NP_055403.2).
    Isotype
    IgG
    Top Product
    Discover our top product VSX1 Primary Antibody
  • Application Notes
    WB 1:500-1:2000
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    1 mg/mL
    Buffer
    PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
    Preservative
    Sodium azide
    Precaution of Use
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Storage
    -20 °C
    Storage Comment
    Store at -20°C. Avoid freeze / thaw cycles.
  • Target
    VSX1 (Visual System Homeobox 1 (VSX1))
    Alternative Name
    VSX1 (VSX1 Products)
    Synonyms
    VSX1 antibody, CAASDS antibody, KTCN antibody, KTCN1 antibody, PPCD antibody, PPD antibody, RINX antibody, CHX10-1 antibody, CHX10-like antibody, visual system homeobox 1 antibody, visual system homeobox 1 L homeolog antibody, visual system homeobox 1 homolog, chx10-like antibody, Vsx1 antibody, VSX1 antibody, Tsp_01485 antibody, vsx1.L antibody, vsx1 antibody
    Background
    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.
    Molecular Weight

    Observed_MW: 40 kDa

    Calculated_MW: 14 kDa/22 kDa/24 kDa/29 kDa/32 kDa/38 kDa/39 kDa

    Gene ID
    30813
    UniProt
    Q9NZR4
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