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L1CAM antibody

This Rabbit Polyclonal antibody specifically detects L1CAM in IHC and ELISA. It exhibits reactivity toward Human, Mouse and Rat.
Catalog No. ABIN7242980

Quick Overview for L1CAM antibody (ABIN7242980)

Target

See all L1CAM Antibodies
L1CAM (L1 Cell Adhesion Molecule (L1CAM))

Reactivity

  • 117
  • 38
  • 36
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
Human, Mouse, Rat

Host

  • 92
  • 34
  • 2
Rabbit

Clonality

  • 77
  • 50
  • 1
Polyclonal

Conjugate

  • 73
  • 13
  • 5
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This L1CAM antibody is un-conjugated

Application

  • 71
  • 44
  • 43
  • 42
  • 25
  • 22
  • 18
  • 14
  • 13
  • 7
  • 6
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
Immunohistochemistry (IHC), ELISA
  • Characteristics

    Polyclonal Antibody

    Purification

    Affinity purification

    Immunogen

    Synthetic peptide of human L1CAM

    Isotype

    IgG
  • Application Notes

    IHC 1:25-1:100

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.3 mg/mL

    Buffer

    PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4

    Preservative

    Sodium azide

    Precaution of Use

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

    Storage

    -20 °C

    Storage Comment

    Store at -20°C. Avoid freeze / thaw cycles.
  • Target

    L1CAM (L1 Cell Adhesion Molecule (L1CAM))

    Alternative Name

    L1CAM

    Background

    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 X-linked neurological syndromes known as CRASH (corpus callosum hypoplasia, retardation, aphasia, spastic paraplegia and hydrocephalus). Alternative splicing of this gene results in multiple transcript variants, some of which include an alternate exon that is considered to be specific to neurons.

    NCBI Accession

    NP_000416

    UniProt

    P32004

    Pathways

    Synaptic Membrane
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