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NEFL antibody (AA 89-400) (Biotin)

The Rabbit Monoclonal anti-NEFL antibody has been validated for ELISA. It is suitable to detect NEFL in samples from Human.
Catalog No. ABIN7608326

Quick Overview for NEFL antibody (AA 89-400) (Biotin) (ABIN7608326)

Target

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

Reactivity

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

Host

  • 89
  • 48
  • 8
  • 1
  • 1
  • 1
Rabbit

Clonality

  • 77
  • 71
Monoclonal

Conjugate

  • 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

Application

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

Clone

DM199
  • Binding Specificity

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

    Purpose

    Biotinylated Anti-NEFL(89-400) antibody(DM199), Rabbit mAb

    Purification

    Purified from cell culture supernatant by affinity chromatography

    Isotype

    IgG
  • Application Notes

    ELISA 1:5000-10000

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Buffer

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

    Storage

    -20 °C,-80 °C

    Storage Comment

    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.

    Expiry Date

    12 months
  • Target

    NEFL (Neurofilament, Light Polypeptide (NEFL))

    Alternative Name

    NEFL

    Background

    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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