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Nyctalopin 抗体 (N-Term)

NYX 适用: 人 WB, EIA 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN953798
发货至: 中国
  • 抗原 See all Nyctalopin (NYX) 抗体
    Nyctalopin (NYX)
    抗原表位
    • 8
    • 7
    • 6
    • 2
    AA 59-89, N-Term
    适用
    • 17
    • 2
    宿主
    • 17
    克隆类型
    • 17
    多克隆
    标记
    • 7
    • 2
    • 2
    • 2
    • 2
    • 2
    This Nyctalopin antibody is un-conjugated
    应用范围
    • 16
    • 14
    • 3
    Western Blotting (WB), Enzyme Immunoassay (EIA)
    特异性
    This antibody recognizes Human Nyctalopin (N-term).
    纯化方法
    Protein A column, followed by peptide affinity purification
    免疫原
    KLH conjugated synthetic peptide between 59~89 amino acids from the N-terminal region of Human Nyctalopin. Genename: NYX
    亚型
    Ig Fraction
    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
    浓度
    0.25 mg/mL
    缓冲液
    PBS containing 0.09 % (W/V) Sodium Azide as preservative
    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.
    注意事项
    Avoid repeated freezing and thawing.
    储存条件
    4 °C/-20 °C
    储存方法
    Store undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.
  • 抗原
    Nyctalopin (NYX)
    别名
    Nyctalopin (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. [provided by RefSeq].Synonyms: CLRP, NYX
    分子量
    52000 Da
    基因ID
    60506
    NCBI登录号
    NP_072089
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