L1CAM monoclonal antibody, clone UJ127

Catalog # MAB11365

Size

Price

Stock

Quantity

Size:100 ug
Price: USD $ 428.00
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

    Mouse monoclonal antibody raised against L1CAM.

    Immunogen

    Homogenous suspension of 16 week human fetal brain.

    Host

    Mouse

    Reactivity

    Human

    Form

    Liquid

    Purification

    Protein A/G affinity chromatography

    Isotype

    IgG1, kappa

    Recommend Usage

    Flow Cytometry (0.5-1 ug/million cells)
    Immunofluorescence (1-2 ug/mL)
    Immunohistochemistry (Frozen sections) (1-2 ug/mL for 30 min at RT)
    Immunoprecipitation (1-2 ug/500 ug protein)
    Western Blot (0.5-1 ug/mL)
    The optimal working dilution should be determined by the end user.

    Storage Buffer

    In PBS, pH 7.4 (0.05% BSA, 0.05% sodium azide)

    Storage Instruction

    Store at 4°C.
    Aliquot to avoid repeated freezing and thawing.

    Note

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

  • Applications

    Western Blot

    Immunohistochemistry (Frozen sections)

    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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