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Nyctalopin antibody (Middle Region)

NYX Reactivity: Human WB Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN5517443
  • Target See all Nyctalopin (NYX) Antibodies
    Nyctalopin (NYX)
    Binding Specificity
    • 8
    • 8
    • 7
    • 2
    Middle Region
    Reactivity
    • 18
    • 2
    Human
    Host
    • 18
    Rabbit
    Clonality
    • 18
    Polyclonal
    Conjugate
    • 8
    • 2
    • 2
    • 2
    • 2
    • 2
    This Nyctalopin antibody is un-conjugated
    Application
    • 17
    • 14
    • 3
    • 1
    Western Blotting (WB)
    Sequence
    GSGRVTDVPC ASPGSVAGLD LSQVTFGRSS DGLCVDPEEL NLTTSSPGPS
    Purification
    Affinity purified
    Immunogen
    The immunogen is a synthetic peptide directed towards the middle region of human NYX
    Top Product
    Discover our top product NYX Primary Antibody
  • Application Notes
    Optimal working dilution should be determined by the investigator.
    Restrictions
    For Research Use only
  • Format
    Liquid
    Buffer
    Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 23 % sucrose.
    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
    For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.
  • Target
    Nyctalopin (NYX)
    Alternative Name
    NYX (NYX Products)
    Synonyms
    MGC84276 antibody, CLRP antibody, CSNB1 antibody, CSNB1A antibody, CSNB4 antibody, NBM1 antibody, CLNP antibody, nob antibody, RGD1561300 antibody, nyctalopin antibody, nyctalopin L homeolog antibody, uncharacterized LOC491837 antibody, NYX antibody, nyx.L antibody, LOC491837 antibody, nyx antibody, Nyx antibody
    Background
    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.

    Alias Symbols: CLRP, NBM1, CSNB1, CSNB4, CSNB1A

    Protein Size: 481
    Gene ID
    60506
    NCBI Accession
    NM_022567, NP_072089
    UniProt
    Q9GZU5
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