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Spastin anticorps

Cet anticorps Lapin Polyclonal détecte spécifiquement Spastin dans ELISA et IHC. Il présente une réactivité envers Souris, Rat et Humain.
N° du produit ABIN7243310

Aperçu rapide pour Spastin anticorps (ABIN7243310)

Antigène

Voir toutes Spastin (SPAST) Anticorps
Spastin (SPAST)

Reactivité

  • 36
  • 36
  • 26
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Souris, Rat, Humain

Hôte

  • 27
  • 15
Lapin

Clonalité

  • 26
  • 16
Polyclonal

Conjugué

  • 12
  • 3
  • 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
  • 1
  • 1
Cet anticorp Spastin est non-conjugé

Application

  • 35
  • 14
  • 13
  • 13
  • 13
  • 8
  • 4
  • 3
  • 2
  • 2
  • 1
  • 1
ELISA, Immunohistochemistry (IHC)
  • Attributs du produit

    Polyclonal Antibody

    Purification

    Affinity purification

    Immunogène

    Synthetic peptide of human SPAST

    Isotype

    IgG
  • Indications d'application

    IHC 1:50-1:200

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.6 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

    Spastin (SPAST)

    Autre désignation

    SPAST

    Sujet

    This gene encodes a member of the AAA (ATPases associated with a variety of cellular activities) protein family. Members of this protein family share an ATPase domain and have roles in diverse cellular processes including membrane trafficking, intracellular motility, organelle biogenesis, protein folding, and proteolysis. The encoded ATPase may be involved in the assembly or function of nuclear protein complexes. Two transcript variants encoding distinct isoforms have been identified for this gene. Other alternative splice variants have been described but their full length sequences have not been determined. Mutations associated with this gene cause the most frequent form of autosomal dominant spastic paraplegia 4.

    NCBI Accession

    NP_055761

    UniProt

    Q9UBP0

    Pathways

    Dynamique des Microtubules, M Phase, Regulation of Cell Size
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