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Nyctalopin anticorps (N-Term)

NYX Reactivité: Humain WB Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN5537867
  • Antigène Voir toutes Nyctalopin (NYX) Anticorps
    Nyctalopin (NYX)
    Épitope
    • 8
    • 8
    • 7
    • 2
    AA 53-80, N-Term
    Reactivité
    • 18
    • 2
    Humain
    Hôte
    • 18
    Lapin
    Clonalité
    • 18
    Polyclonal
    Conjugué
    • 8
    • 2
    • 2
    • 2
    • 2
    • 2
    Cet anticorp Nyctalopin est non-conjugé
    Application
    • 17
    • 14
    • 3
    • 1
    Western Blotting (WB)
    Purification
    This antibody is purified through a protein A column, followed by peptide affinity purification.
    Immunogène
    This NYX antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 53-80 amino acids from the N-terminal region of human NYX.
    Isotype
    Ig Fraction
    Top Product
    Discover our top product NYX Anticorps primaire
  • Indications d'application
    For WB starting dilution is: 1:1000
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    0.5 mg/mL
    Buffer
    Supplied in PBS with 0.09 % (W/V) sodium azide.
    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
    4 °C,-20 °C
    Stockage commentaire
    Store at 4°C for three months and -20°C, stable for up to one year. As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.
  • Antigène
    Nyctalopin (NYX)
    Autre désignation
    NYX (NYX Produits)
    Synonymes
    anticorps MGC84276, anticorps CLRP, anticorps CSNB1, anticorps CSNB1A, anticorps CSNB4, anticorps NBM1, anticorps CLNP, anticorps nob, anticorps RGD1561300, anticorps nyctalopin, anticorps nyctalopin L homeolog, anticorps uncharacterized LOC491837, anticorps NYX, anticorps nyx.L, anticorps LOC491837, anticorps nyx, anticorps Nyx
    Sujet
    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. [provided by RefSeq].
    Poids moléculaire
    52 kDa
    ID gène
    60506
    UniProt
    Q9GZU5
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