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NEFH 抗体 (AA 109-466)

The 兔 多克隆 anti-NEFH antibody (ABIN7870057) specifically detects NEFH in WB, FACS, ELISA 和 IHC (p). The antibody is reactive with 大鼠 和 小鼠 samples.
产品编号 ABIN7870057
发货至: 中国
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Quick Overview for NEFH 抗体 (AA 109-466) (ABIN7870057)

抗原

See all NEFH 抗体
NEFH (Neurofilament, Heavy Polypeptide (NEFH))

适用

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  • 102
  • 86
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  • 13
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  • 9
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  • 2
  • 2
  • 1
  • 1
大鼠, 小鼠

宿主

  • 73
  • 73
  • 9

克隆类型

  • 101
  • 54
多克隆

标记

  • 96
  • 6
  • 4
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  • 2
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  • 1
  • 1
  • 1
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  • 1
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  • 1
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This NEFH antibody is un-conjugated

应用范围

  • 109
  • 79
  • 42
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  • 14
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  • 11
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  • 2
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  • 1
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Western Blotting (WB), Flow Cytometry (FACS), ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
  • 抗原表位

    • 16
    • 12
    • 10
    • 4
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 109-466

    原理

    Neurofilament heavy Antibody / Nefh

    纯化方法

    Affinity purified

    免疫原

    A mouse recombinant partial protein (amino acids Y109-E466) was used as the immunogen for the Neurofilament heavy antibody.

    亚型

    IgG
  • 应用备注

    Optimal dilution of the Neurofilament heavy antibody should be determined by the researcher.

    限制

    仅限研究用
  • 状态

    Lyophilized

    缓冲液

    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

    储存条件

    4 °C,-20 °C

    储存方法

    After reconstitution, the Neurofilament heavy antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
  • 抗原

    NEFH (Neurofilament, Heavy Polypeptide (NEFH))

    别名

    Neurofilament heavy

    背景

    Neurofilaments are type IV intermediate filament heteropolymers composed of light, medium, and heavy chains. Neurofilaments comprise the axoskeleton and functionally maintain neuronal caliber. They may also play a role in intracellular transport to axons and dendrites. This gene encodes the heavy neurofilament protein. This protein is commonly used as a biomarker of neuronal damage and susceptibility to amyotrophic lateral sclerosis (ALS) has been associated with mutations in this gene.

    UniProt

    P19246
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