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L1CAM anticorps

Cet anticorps Lapin Polyclonal détecte spécifiquement L1CAM dans IHC et ELISA. Il présente une réactivité envers Humain, Souris et Rat.
N° du produit ABIN7242980

Aperçu rapide pour L1CAM anticorps (ABIN7242980)

Antigène

Voir toutes L1CAM Anticorps
L1CAM (L1 Cell Adhesion Molecule (L1CAM))

Reactivité

  • 112
  • 39
  • 34
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
Humain, Souris, Rat

Hôte

  • 84
  • 34
  • 2
Lapin

Clonalité

  • 71
  • 48
  • 1
Polyclonal

Conjugué

  • 66
  • 12
  • 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
Cet anticorp L1CAM est non-conjugé

Application

  • 64
  • 43
  • 43
  • 33
  • 25
  • 17
  • 14
  • 13
  • 11
  • 7
  • 6
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
Immunohistochemistry (IHC), ELISA
  • Attributs du produit

    Polyclonal Antibody

    Purification

    Affinity purification

    Immunogène

    Synthetic peptide of human L1CAM

    Isotype

    IgG
  • Indications d'application

    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

    Agent conservateur

    Sodium azide

    Précaution d'utilisation

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

    Stock

    -20 °C

    Stockage commentaire

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

    L1CAM (L1 Cell Adhesion Molecule (L1CAM))

    Autre désignation

    L1CAM

    Sujet

    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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