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ATL1 anticorps

Cet anticorps anti-ATL1 Polyclonal Lapin (ABIN7880014) détecte spécifiquement ATL1 dans WB, IHC (p) et FACS. L’anticorps est réactif avec des échantillons de Humain.
N° du produit ABIN7880014
644,88 €
Plus frais de livraison 40,00 € et TVA
100 μg
Destination: France
Envoi sous 6 à 9 jours ouvrables

Aperçu rapide pour ATL1 anticorps (ABIN7880014)

Antigène

Voir toutes ATL1 Anticorps
ATL1 (Atlastin GTPase 1 (ATL1))

Reactivité

  • 32
  • 20
  • 19
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
Humain

Hôte

  • 44
  • 3
Lapin

Clonalité

  • 44
  • 3
Polyclonal

Conjugué

  • 18
  • 4
  • 3
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp ATL1 est non-conjugé

Application

  • 35
  • 20
  • 13
  • 13
  • 3
  • 3
  • 3
  • 3
  • 3
  • 2
  • 1
Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Flow Cytometry (FACS)
  • Fonction

    Atlastin-1 Antibody / ATL1 / SPG3A

    Séquence

    DKPFLAPNDL QTKHLQ

    Purification

    Antigen affinity purified

    Immunogène

    Amino acids DKPFLAPNDLQTKHLQ from the human protein were used as the immunogen for the Atlastin-1 antibody.

    Isotype

    IgG
  • Indications d'application

    Optimal dilution of the Atlastin-1 antibody should be determined by the researcher.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Buffer

    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

    Stock

    4 °C,-20 °C

    Stockage commentaire

    After reconstitution, the Atlastin-1 antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
  • Antigène

    ATL1 (Atlastin GTPase 1 (ATL1))

    Autre désignation

    Atlastin-1

    Sujet

    Atlastin, or Atlastin-1, is a protein that in humans is encoded by the ATL1 gene. The protein encoded by this gene is a GTPase and a Golgi body transmembrane protein. The encoded protein can form a homotetramer and has been shown to interact with spastin and with mitogen-activated protein kinase kinase kinase kinase 4. This protein may be involved in axonal maintenance as evidenced by the fact that defects in this gene are a cause of spastic paraplegia type 3. Three transcript variants encoding two different isoforms have been found for this gene.

    UniProt

    Q8WXF7
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