L1CAM (phospho S1181) polyclonal antibody

Catalog # PAB31655

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Size:100 uL
Price: USD $ 346.00
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Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
  • Specification

    Product Description

    Rabbit polyclonal antibody raised against synthetic peptide of human L1CAM (phospho S1181).

    Immunogen

    A synthetic peptide corresponding to amino acids 1120-1200 of human L1CAM (phospho S1181).

    Host

    Rabbit

    Reactivity

    Human, Mouse, Rat

    Specificity

    This antibody detects endogenous levels of L1CAM protein only when phosphorylated at S1181.

    Form

    Liquid

    Purification

    Affinity purification

    Isotype

    IgG

    Recommend Usage

    ELISA (1:20000)
    Immunohistochemistry (1:100-300)
    Western Blot (1:500-2000)
    The optimal working dilution should be determined by the end user.

    Storage Buffer

    In PBS (50% glycerol, 0.5% BSA and 0.02% sodium azide).

    Storage Instruction

    Store at -20°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

    Enzyme-linked Immunoabsorbent Assay

  • Gene Info — L1CAM

    Entrez GeneID

    3897

    Protein Accession#

    P32004

    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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