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PLP1 anticorps

Cet anticorps Lapin Polyclonal détecte spécifiquement PLP1 dans WB. Il présente une réactivité avec des échantillons de Humain, Rat, Souris et Chien.
N° du produit ABIN635572
1.309,82 €
Plus frais de livraison 40,00 € et TVA
100 μL
Destination: France
Envoi sous 13 à 17 jours ouvrables

Aperçu rapide pour PLP1 anticorps (ABIN635572)

Antigène

Voir toutes PLP1 Anticorps
PLP1 (Proteolipid Protein 1 (PLP1))

Reactivité

  • 37
  • 29
  • 13
  • 10
  • 9
  • 4
  • 3
  • 3
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
Humain, Rat, Souris, Chien

Hôte

  • 38
  • 13
  • 3
Lapin

Clonalité

  • 42
  • 12
Polyclonal

Conjugué

  • 30
  • 3
  • 3
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp PLP1 est non-conjugé

Application

  • 43
  • 19
  • 17
  • 13
  • 13
  • 12
  • 11
  • 7
  • 7
  • 5
  • 1
  • 1
  • 1
Western Blotting (WB)
  • Purification

    Affinity purified

    Immunogène

    PLP1 antibody was raised using a synthetic peptide corresponding to a region with amino acids GHEALTGTEKLIETYFSKNYQDYEYLINVIHAFQYVIYGTASFFFLYGAL
  • Indications d'application

    WB: 1 µg/mL
    Optimal conditions should be determined by the investigator.

    Commentaires

    PLP1 Blocking Peptide, (ABIN938693), is also available for use as a blocking control in assays to test for specificity of this PLP1 antibody

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

    Lyophilized powder. Add distilled water for a 1 mg/mL concentration of PLP1 antibody in PBS

    Concentration

    Lot specific

    Buffer

    PBS

    Conseil sur la manipulation

    Avoid repeated freeze/thaw cycles.

    Stock

    4 °C/-20 °C

    Stockage commentaire

    Store at 2-8 °C for short periods. For longer periods of storage, store at -20 °C.
  • Antigène

    PLP1 (Proteolipid Protein 1 (PLP1))

    Autre désignation

    PLP1

    Sujet

    PLP1 is a transmembrane proteolipid protein that is the predominant myelin protein present in the central nervous system. It may play a role in the compaction, stabilization, and maintenance of myelin sheaths, as well as in oligodendrocyte development and axonal survival. Mutations in this gene cause X-linked Pelizaeus-Merzbacher disease and spastic paraplegia type 2. Alternatively spliced transcript variants encoding distinct isoforms or having different 5' UTRs, have been identified for this gene.

    Poids moléculaire

    30 kDa (MW of target protein)
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