L1CAM recombinant monoclonal antibody, clone L1-14.10

Catalog # RAB03175

Size

Price

Stock

Quantity

Size:200 ug
Price: USD $ 850.00
Stock:
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Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
  • Specification

    Product Description

    Rabbit recombinant monoclonal antibody raised against human L1CAM.Recombinant Antibody,Recombinant Antibodies,Recombinant Monoclonal Antibody,RecomAb,Recombinant Ab,Recombinant Monoclonal Antibodies,Recombinant Abs

    Antibody Species

    Rabbit

    Immunogen

    Original antibody is raised against recombinant L1-Fc fusion protein, consisting of the ectodomain of human L1.

    Reactivity

    Human

    Form

    Liquid

    Isotype

    IgG

    Recommend Usage

    Flow Cytometry
    Immunofluorescence
    Immunohistochemistry
    Immunoprecipitation
    Western Blot
    The optimal working dilution should be determined by the end user.

    Storage Buffer

    In PBS with 0.02% Proclin 300

    Storage Instruction

    Store at 4°C for up to 3 months. For longer storage, aliquot and store at -20°C.
    Aliquot to avoid repeated freezing and thawing.

  • Applications

    Western Blot

    Immunohistochemistry

    Immunofluorescence

    Immunoprecipitation

    Flow Cytometry

  • Gene Info — L1CAM

    Entrez GeneID

    3897

    Gene Name

    L1CAM

    Gene Alias

    CAML1, CD171, HSAS, HSAS1, MASA, MIC5, N-CAML1, S10, SPG1

    Gene Description

    L1 cell adhesion molecule

    Omim ID

    142623 303350 304100 307000 308840

    Gene Ontology

    Hyperlink

    Gene Summary

    The protein encoded by this gene is an axonal glycoprotein belonging to the immunoglobulin supergene family. The ectodomain, consisting of several immunoglobulin-like domains and fibronectin-like repeats (type III), is linked via a single transmembrane sequence to a conserved cytoplasmic domain. This cell adhesion molecule plays an important role in nervous system development, including neuronal migration and differentiation. Mutations in the gene cause three X-linked neurological syndromes known by the acronym CRASH (corpus callosum hypoplasia, retardation, aphasia, spastic paraplegia and hydrocephalus). Alternative splicing of a neuron-specific exon is thought to be functionally relevant. [provided by RefSeq

    Other Designations

    OTTHUMP00000025992|antigen identified by monoclonal antibody R1|neural cell adhesion molecule L1

  • 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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