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Recombinant Human Neurofilament light polypeptide (NEFL),Truncated

ACP01061

Number
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Specifications


Cat.No ACP01061 Target NameNEFL
Target Synonyms(NF-L)(68 kDa neurofilament protein)(Neurofilament triplet L protein)FormLiquid or Lyophilized powder
Expression SystemE.coliExpression Range50-400aa
Mol Weight52.4 kDaProtein LengthPartial
PurityGreater than 85% as determined by SDS-PAGE.Storage Buffer5%-50% glycerol. Lyophilized powder form: the buffer before lyophilization is Tris/PBS-based buffer, 6% Trehalose, Liquid form: default storage buffer is Tris/PBS-based buffer, pH 8.0.

Immunogen Information


Target SpeciesHumanUniprot IDP07196
Background Information
  • Uniprot Id

    P07196

  • Target Species

    Human

  • Target Name

    NEFL

  • Target Full Name

    Neurofilament light polypeptide

  • Target Function

    Neurofilaments usually contain three intermediate filament proteins: NEFL, NEFM, and NEFH which are involved in the maintenance of neuronal caliber. May additionally cooperate with the neuronal intermediate filament proteins PRPH and INA to form neuronal filamentous networks.

  • Target Involvement

    Charcot-Marie-Tooth disease 1F (CMT1F); Charcot-Marie-Tooth disease 2E (CMT2E)

  • Target Subcellular Location

    Cell projection, axon. Cytoplasm, cytoskeleton.

  • Target Protein Families

    Intermediate filament family

  • Target Research Area

    Others

  • Target Synonyms

    NEFL; NF68; NFL; Neurofilament light polypeptide; NF-L; 68 kDa neurofilament protein; Neurofilament triplet L protein

  • Target 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.

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