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NEFL 抗体 (AA 89-400) (Biotin)

This anti-NEFL antibody is a 兔 单克隆 antibody detecting NEFL in ELISA. Suitable for 人.
产品编号 ABIN7608324
发货至: 中国

Quick Overview for NEFL 抗体 (AA 89-400) (Biotin) (ABIN7608324)

抗原

See all NEFL 抗体
NEFL (Neurofilament, Light Polypeptide (NEFL))

适用

  • 111
  • 52
  • 45
  • 27
  • 24
  • 18
  • 4
  • 2
  • 2
  • 2
  • 1
  • 1

宿主

  • 89
  • 48
  • 8
  • 1
  • 1
  • 1

克隆类型

  • 77
  • 71
单克隆

标记

  • 100
  • 18
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This NEFL antibody is conjugated to Biotin

应用范围

  • 90
  • 72
  • 42
  • 34
  • 33
  • 32
  • 26
  • 16
  • 14
  • 13
  • 11
  • 10
  • 4
  • 3
  • 2
  • 2
  • 1
  • 1
ELISA

克隆位点

6C5
  • 抗原表位

    • 15
    • 7
    • 6
    • 5
    • 4
    • 4
    • 3
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 89-400

    原理

    Biotinylated Anti-NEFL(89-400) antibody(6C5), Rabbit mAb

    纯化方法

    Purified from cell culture supernatant by affinity chromatography

    亚型

    IgG
  • 应用备注

    ELISA 1:5000-10000

    限制

    仅限研究用
  • 状态

    Lyophilized

    缓冲液

    Lyophilized from sterile PBS, pH 7.4. Normally 5 % - 8 % trehalose is added as protectants before lyophilization.

    储存条件

    -20 °C,-80 °C

    储存方法

    Store at -20°C to -80°C for 12 months in lyophilized form. After reconstitution, if not intended for use within a month, aliquot and store at -80°C (Avoid repeated freezing and thawing). Lyophilized proteins are shipped at ambient temperature.

    有效期

    12 months
  • 抗原

    NEFL (Neurofilament, Light Polypeptide (NEFL))

    别名

    NEFL

    背景

    Neurofilaments are type IV intermediate filament heteropolymers composed of light, medium, and heavy chains. Neurofilaments comprise the axoskeleton and they functionally maintain the neuronal caliber. They may also play a role in intracellular transport to axons and dendrites. This gene encodes the light chain neurofilament protein. Mutations in this gene cause Charcot-Marie-Tooth disease types 1F (CMT1F) and 2E (CMT2E), disorders of the peripheral nervous system that are characterized by distinct neuropathies. A pseudogene has been identified on chromosome Y.

    UniProt

    P07196
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