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Nyctalopin Antikörper

NYX Reaktivität: Human, Maus IHC Wirt: Kaninchen Polyclonal unconjugated
Produktnummer ABIN6571393
  • Target Alle Nyctalopin (NYX) Antikörper anzeigen
    Nyctalopin (NYX)
    Reaktivität
    Human, Maus
    Wirt
    • 18
    Kaninchen
    Klonalität
    • 18
    Polyklonal
    Konjugat
    • 8
    • 2
    • 2
    • 2
    • 2
    • 2
    Dieser Nyctalopin Antikörper ist unkonjugiert
    Applikation
    • 17
    • 14
    • 3
    • 1
    Immunohistochemistry (IHC)
    Aufreinigung
    Affinity purification
    Immunogen
    Recombinant fusion protein of human NYX (NP_072089.1).
    Isotyp
    IgG
    Top Product
    Discover our top product NYX Primärantikörper
  • Applikationshinweise
    IHC 1:50-1:100
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Liquid
    Konzentration
    1 mg/mL
    Buffer
    PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
    Konservierungsmittel
    Sodium azide
    Vorsichtsmaßnahmen
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Lagerung
    -20 °C
    Informationen zur Lagerung
    Store at -20°C. Avoid freeze / thaw cycles.
  • Target
    Nyctalopin (NYX)
    Andere Bezeichnung
    NYX (NYX Produkte)
    Synonyme
    MGC84276 antikoerper, CLRP antikoerper, CSNB1 antikoerper, CSNB1A antikoerper, CSNB4 antikoerper, NBM1 antikoerper, CLNP antikoerper, nob antikoerper, RGD1561300 antikoerper, nyctalopin antikoerper, nyctalopin L homeolog antikoerper, uncharacterized LOC491837 antikoerper, NYX antikoerper, nyx.L antikoerper, LOC491837 antikoerper, nyx antikoerper, Nyx antikoerper
    Hintergrund
    The product of this gene belongs to the small leucine-rich proteoglycan (SLRP) family of proteins. Defects in this gene are the cause of congenital stationary night blindness type 1 (CSNB1), also called X-linked congenital stationary night blindness (XLCSNB). CSNB1 is a rare inherited retinal disorder characterized by impaired scotopic vision, myopia, hyperopia, nystagmus and reduced visual acuity. The role of other SLRP proteins suggests that mutations in this gene disrupt developing retinal interconnections involving the ON-bipolar cells, leading to the visual losses seen in patients with complete CSNB.
    Molekulargewicht

    Observed_MW: 52kDa

    Calculated_MW: 52kDa

    Gen-ID
    60506
    UniProt
    Q9GZU5
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