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Nyctalopin 抗体 (Middle Region)

NYX 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN5517443
发货至: 中国
  • 抗原 See all Nyctalopin (NYX) 抗体
    Nyctalopin (NYX)
    抗原表位
    • 8
    • 8
    • 7
    • 2
    Middle Region
    适用
    • 18
    • 2
    宿主
    • 18
    克隆类型
    • 18
    多克隆
    标记
    • 8
    • 2
    • 2
    • 2
    • 2
    • 2
    This Nyctalopin antibody is un-conjugated
    应用范围
    • 17
    • 14
    • 3
    • 1
    Western Blotting (WB)
    序列
    GSGRVTDVPC ASPGSVAGLD LSQVTFGRSS DGLCVDPEEL NLTTSSPGPS
    纯化方法
    Affinity purified
    免疫原
    The immunogen is a synthetic peptide directed towards the middle region of human NYX
    Top Product
    Discover our top product NYX Primary Antibody
  • 应用备注
    Optimal working dilution should be determined by the investigator.
    限制
    仅限研究用
  • 状态
    Liquid
    缓冲液
    Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 23 % sucrose.
    储存液
    Sodium azide
    注意事项
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    储存条件
    -20 °C
    储存方法
    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.
  • 抗原
    Nyctalopin (NYX)
    别名
    NYX (NYX 产品)
    别名
    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
    背景
    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
    基因ID
    60506
    NCBI登录号
    NM_022567, NP_072089
    UniProt
    Q9GZU5
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