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NEFL antibody

This anti-NEFL antibody is a Mouse Monoclonal antibody detecting NEFL in WB, IF, FACS, IHC (p) and EIA. Suitable for Human.
Catalog No. ABIN1108416

Quick Overview for NEFL antibody (ABIN1108416)

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

  • 90
  • 47
  • 8
  • 1
  • 1
  • 1
Mouse

Clonality

  • 77
  • 71
Monoclonal

Conjugate

  • 99
  • 19
  • 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 un-conjugated

Application

  • 89
  • 72
  • 42
  • 33
  • 33
  • 33
  • 25
  • 15
  • 14
  • 13
  • 11
  • 10
  • 4
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  • 2
  • 1
Western Blotting (WB), Immunofluorescence (IF), Flow Cytometry (FACS), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Enzyme Immunoassay (EIA)

Clone

1H3
  • Specificity

    This antibody reacts to NEFL.

    Cross-Reactivity (Details)

    Species reactivity (tested):Human.

    Purification

    Purified

    Isotype

    IgG1
  • Application Notes

    Optimal working dilution should be determined by the investigator.

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1.0 mg/mL

    Buffer

    PBS, 0.05 % sodium azide, 0,5 % BSA

    Preservative

    Sodium azide

    Precaution of Use

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

    NEFL (Neurofilament, Light Polypeptide (NEFL))

    Alternative Name

    Neurofilament L (68kDa)

    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.Synonyms: 68 kDa neurofilament protein, NEFL, NF-L, NF68, Neurofilament L

    Molecular Weight

    62 kDa

    Gene ID

    4747
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