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Nyctalopin 抗体 (AA 282-481)

NYX 适用: 人 WB, IHC 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN6144979
发货至: 中国
  • 抗原 See all Nyctalopin (NYX) 抗体
    Nyctalopin (NYX)
    抗原表位
    • 8
    • 8
    • 7
    • 2
    AA 282-481
    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), Immunohistochemistry (IHC)
    序列
    LLYLDRNSIA FVEEGAFQNL SGLLALHLNG NRLTVLAWVA FQPGFFLGRL FLFRNPWCCD CRLEWLRDWM EGSGRVTDVP CASPGSVAGL DLSQVTFGRS SDGLCVDPEE LNLTTSSPGP SPEPAATTVS RFSSLLSKLL APRVPVEEAA NTTGGLANAS LSDSLSSRGV GGAGRQPWFL LASCLLPSVA QHVVFGLQMD
    交叉反应
    人, 小鼠
    产品特性
    Polyclonal Antibodies
    免疫原
    Recombinant fusion protein containing a sequence corresponding to amino acids 282-481 of human NYX (NP_072089.1).
    亚型
    IgG
    Top Product
    Discover our top product NYX Primary Antibody
  • 应用备注
    WB,1:500 - 1:2000,IHC,1:50 - 1:100
    说明

    HIGH QUALITY

    限制
    仅限研究用
  • 状态
    Liquid
    缓冲液
    PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.
    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
    Store at -20°C. Avoid 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.,NYX,CLRP,CSNB1,CSNB1A,CSNB4,NBM1,Neuroscience,NYX
    分子量
    52 kDa
    基因ID
    60506
    UniProt
    Q9GZU5
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