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VSX1 anticorps

VSX1 Reactivité: Humain WB Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN7264858
  • Antigène Voir toutes VSX1 Anticorps
    VSX1 (Visual System Homeobox 1 (VSX1))
    Reactivité
    • 31
    • 7
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    Humain
    Hôte
    • 33
    Lapin
    Clonalité
    • 33
    Polyclonal
    Conjugué
    • 16
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp VSX1 est non-conjugé
    Application
    • 26
    • 15
    • 1
    Western Blotting (WB)
    Attributs du produit
    Polyclonal Antibody
    Purification
    Affinity purification
    Immunogène
    Recombinant fusion protein of human VSX1 (NP_055403.2).
    Isotype
    IgG
    Top Product
    Discover our top product VSX1 Anticorps primaire
  • Indications d'application
    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
    Agent conservateur
    Sodium azide
    Précaution d'utilisation
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Stock
    -20 °C
    Stockage commentaire
    Store at -20°C. Avoid freeze / thaw cycles.
  • Antigène
    VSX1 (Visual System Homeobox 1 (VSX1))
    Autre désignation
    VSX1 (VSX1 Produits)
    Synonymes
    anticorps VSX1, anticorps CAASDS, anticorps KTCN, anticorps KTCN1, anticorps PPCD, anticorps PPD, anticorps RINX, anticorps CHX10-1, anticorps CHX10-like, anticorps visual system homeobox 1, anticorps visual system homeobox 1 L homeolog, anticorps visual system homeobox 1 homolog, chx10-like, anticorps Vsx1, anticorps VSX1, anticorps Tsp_01485, anticorps vsx1.L, anticorps vsx1
    Sujet
    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.
    Poids moléculaire

    Observed_MW: 40 kDa

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

    ID gène
    30813
    UniProt
    Q9NZR4
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