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NEFL antibody

This Rabbit Polyclonal antibody specifically detects NEFL in IHC and IF. It exhibits reactivity toward Human, Rat and Mouse.
Catalog No. ABIN6566538

Quick Overview for NEFL antibody (ABIN6566538)

Target

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

Reactivity

  • 84
  • 53
  • 52
  • 24
  • 23
  • 18
  • 4
  • 2
  • 2
  • 1
  • 1
  • 1
Human, Rat, Mouse

Host

  • 78
  • 35
  • 7
  • 1
  • 1
  • 1
Rabbit

Clonality

  • 68
  • 55
Polyclonal

Conjugate

  • 73
  • 12
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 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 un-conjugated

Application

  • 75
  • 60
  • 30
  • 27
  • 25
  • 24
  • 19
  • 14
  • 14
  • 13
  • 11
  • 8
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
Immunohistochemistry (IHC), Immunofluorescence (IF)
  • Purification

    Affinity purification

    Immunogen

    Recombinant fusion protein of human NEFL (NP_006149.2).

    Isotype

    IgG
  • Application Notes

    IHC 1:50-1:200 IF 1:50-1:200

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 mg/mL

    Buffer

    PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3

    Preservative

    Sodium azide

    Precaution of Use

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Storage

    -20 °C

    Storage Comment

    Store at -20°C. Avoid freeze / thaw cycles.
  • 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.

    Molecular Weight

    Observed_MW: 82kDa

    Calculated_MW: 61kDa

    Gene ID

    4747

    UniProt

    P07196
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