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Nyctalopin 抗体 (N-Term)

This anti-Nyctalopin antibody is a 兔 多克隆 antibody detecting Nyctalopin in WB. Suitable for 人.
产品编号 ABIN653436
发货至: 中国

Quick Overview for Nyctalopin 抗体 (N-Term) (ABIN653436)

抗原

See all Nyctalopin (NYX) 抗体
Nyctalopin (NYX)

适用

  • 11
  • 1

宿主

  • 11

克隆类型

  • 11
多克隆

标记

  • 6
  • 1
  • 1
  • 1
  • 1
  • 1
This Nyctalopin antibody is un-conjugated

应用范围

  • 11
  • 9
  • 2
  • 1
Western Blotting (WB)

克隆位点

RB23621
  • 抗原表位

    • 7
    • 2
    • 2
    • 2
    AA 53-80, N-Term

    纯化方法

    This antibody is purified through a protein A column, followed by peptide affinity purification.

    免疫原

    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.

    亚型

    Ig Fraction
  • 应用备注

    WB: 1:1000

    限制

    仅限研究用
  • 状态

    Liquid

    缓冲液

    Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.

    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

    4 °C,-20 °C

    储存方法

    Maintain refrigerated at 2-8 °C for up to 6 months. For long term storage store at -20 °C in small aliquots to prevent freeze-thaw cycles.

    有效期

    6 months
  • 抗原

    Nyctalopin (NYX)

    别名

    NYX

    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].

    分子量

    52000

    基因ID

    60506

    NCBI登录号

    NP_072089

    UniProt

    Q9GZU5
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