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CNTNAP2 anticorps (C-Term, Intracellular)

L’anticorps anti-CNTNAP2 Polyclonal Lapin est utilisé pour la détection de CNTNAP2 dans des échantillons de Humain. Il a été validé pour WB, IHC et IF.
N° du produit ABIN7043084
977,85 €
Plus frais de livraison 40,00 € et TVA
Destination: France
Envoi sous 8 à 9 jours ouvrables

Aperçu rapide pour CNTNAP2 anticorps (C-Term, Intracellular) (ABIN7043084)

Antigène

Voir toutes CNTNAP2 Anticorps
CNTNAP2 (Contactin Associated Protein-Like 2 (CNTNAP2))

Reactivité

  • 54
  • 23
  • 8
Humain

Hôte

  • 45
  • 10
Lapin

Clonalité

  • 46
  • 9
Polyclonal

Conjugué

  • 22
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp CNTNAP2 est non-conjugé

Application

  • 44
  • 17
  • 16
  • 11
  • 8
  • 3
  • 3
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (IHC), Immunofluorescence (IF)
  • Épitope

    • 16
    • 8
    • 6
    • 4
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 1315-1331, C-Term, Intracellular

    Fonction

    A Rabbit Polyclonal Antibody to Caspr2

     Réactivité croisée

    Humain, Souris, Rat

    Homologie

    Mouse,rat - identical

    Attributs du produit

    Anti-Caspr2 Antibody is directed against an epitope of human Caspr2. Anti-Caspr2 Antibody (ABIN7043084, ABIN7045145 and ABIN7045146) can be used in western blot and immunohistochemistry analysis. It has been designed to recognize Caspr2 from rat, mouse and human samples.

    Purification

    Affinity purified on immobilized antigen.

    Immunogène

    (C)DPNFTETIDESKKEWLI, corresponding to amino acid residues 1315-1331 of human Caspr2

    Isotype

    IgG
  • Indications d'application

    WB: 1:200

    FC: The optimal concentration should be determined by the user

    ICC: The optimal concentration should be determined by the user

    IHC: 1:200

    IP: The optimal concentration should be determined by the user

    Commentaires

    Negative Control: (ABIN7566011)

    Blocking Peptide: (ABIN7566011)

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

    25 μL, 50 μL or 0.2 mL double distilled water (DDW), depending on the sample size.

    Concentration

    0.8 mg/mL

    Buffer

    PBS pH 7.4, 1 % BSA with 0.05 % sodium azide

    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

    The antibody ships as a lyophilized powder at room temperature. Upon arrival, it should be stored at -20°C
  • Antigène

    CNTNAP2 (Contactin Associated Protein-Like 2 (CNTNAP2))

    Autre désignation

    CNTNAP2

    Sujet

    Synonyms: Contactin-associated protein-like 2, CNTNAP2

    Description: Contactin-associated protein 2 (Caspr2) is a member of the neurexin superfamily, a group of transmembrane proteins that mediate cell-to-cell interactions in the nervous system1,2.Neurexins are adhesion molecules expressed mainly at presynaptic locations that form trans-synaptic cell-to-cell adhesion complexes via binding to their postsynaptic partners, the neuroligins2.Caspr2, like other neurexin proteins, is a type I membrane protein that contains epidermal growth factor repeats, laminin G domains, an F5/8 type C domain, and fibrinogen-like domains in its extracellular domain1,2.Caspr2 is localized at the juxtaparanodes of myelinated axons, a specialized region that mediates interactions between neurons and glia during nervous system development1.The juxtaparanodal region is highly enriched with heteromultimers of the K+ channels KV1.1, KV1.2, and their cytoplasmic KVβ2 subunit, which may help in axon conduction stabilization and the maintenance of the internodal resting potential1. Caspr2 is essential for the targeted localization of these channels in the juxtaparanodal regions. Indeed, targeted disruption of Caspr2 resulted in a marked reduction in the accumulation of K+ channels at the juxtaparanodes in both peripheral and central nervous system axons3.Moreover, mutations in the Caspr2 gene have been implicated in multiple neurodevelopmental disorders, including Tourette syndrome, schizophrenia, epilepsy, autism, attention-deficit hyperactivity disorder and mental retardation4-6.

    ID gène

    26047

    NCBI Accession

    NM_014141

    UniProt

    Q9UHC6
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