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NEFL antibody

This Rabbit Polyclonal antibody specifically detects NEFL in WB, IHC, IF, ELISA and IP. It exhibits reactivity toward Human, Rat and Mouse.
Catalog No. ABIN5699797

Quick Overview for NEFL antibody (ABIN5699797)

Target

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

Reactivity

  • 111
  • 51
  • 44
  • 27
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  • 18
  • 4
  • 2
  • 2
  • 2
  • 1
  • 1
Human, Rat, Mouse

Host

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

Clonality

  • 76
  • 72
Polyclonal

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
  • 71
  • 42
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  • 32
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  • 16
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  • 4
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  • 2
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (IHC), Immunofluorescence (IF), ELISA, Immunoprecipitation (IP)
  • Immunogen

    neurofilament, light polypeptide

    Isotype

    IgG
  • Application Notes

    WB : 1:1000-1:10000 IP :1:500-1:5000 IHC : 1:20-1:400 IF : 1:20-1:200

    Comment

    mouse brain tissue were subjected to SDS PAGE followed by western blot with FNab05710(NEFL antibody) at dilution of 1:4000

    Restrictions

    For Research Use only
  • Buffer

    PBS with 0.02 % sodium azide and 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.

    Handling Advice

    Avoid repeated freeze / thaw cycles.

    Storage

    -20 °C

    Expiry Date

    12 months
  • Target

    NEFL (Neurofilament, Light Polypeptide (NEFL))

    Alternative Name

    NF-L

    Background

    Synonyms:68 kDa neurofilament protein, CMT1F, CMT2E, FLJ53642, NEFL, NF L, NF68, NFL 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

    65-68 kDa,140-160 kDa

    UniProt

    P07196
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