NEFL recombinant monoclonal antibody, clone NEFL/2983R

Catalog # RAB00593

Size

Price

Stock

Quantity

Size:100 ug
Price: USD $ 479.00
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Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
Images
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
Application

Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)

Immunohistochemical staining of human cerebellum.

  • Specification

    Product Description

    Rabbit recombinant monoclonal antibody raised against full length human NEFL.Recombinant Antibody,Recombinant Antibodies,Recombinant Monoclonal Antibody,RecomAb,Recombinant Ab,Recombinant Monoclonal Antibodies,Recombinant Abs

    Antibody Species

    Rabbit

    Immunogen

    Recombinant protein corresponding to full-length human NEFL.

    Reactivity

    Bovine, Chicken, Human, Pig, Rat

    Form

    Liquid

    Purification

    Protein A/G purification

    Isotype

    IgG

    Recommend Usage

    Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) (0.25-0.5 ug/mL)
    The optimal working dilution should be determined by the end user.

    Storage Buffer

    In 1 mg/mL PBS

    Storage Instruction

    Store at -20 to -80°C.

  • Applications

    Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)

    Immunohistochemical staining of human cerebellum.
  • Gene Info — NEFL

    Entrez GeneID

    4747

    Protein Accession#

    P07196

    Gene Name

    NEFL

    Gene Alias

    CMT1F, CMT2E, FLJ53642, NF-L, NF68, NFL

    Gene Description

    neurofilament, light polypeptide

    Omim ID

    162280 607684 607734

    Gene Ontology

    Hyperlink

    Gene Summary

    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. [provided by RefSeq

    Other Designations

    light molecular weight neurofilament protein|neurofilament protein, light chain|neurofilament subunit NF-L|neurofilament triplet L protein|neurofilament, light polypeptide 68kDa|neurofilament-light

  • Interactome
  • Pathway
  • Disease
Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
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