Tel:
+49 (0)241 95 163 153
Fax:
+49 (0)241 95 163 155
E-Mail:
orders@anticorps-enligne.fr

SLMAP anticorps (AA 25-607)

Cet anticorps anti-SLMAP Polyclonal Lapin (ABIN7872886) détecte spécifiquement SLMAP dans WB, ELISA et FACS. L’anticorps est réactif avec des échantillons de Humain et Souris.
N° du produit ABIN7872886
644,88 €
Plus frais de livraison 40,00 € et TVA
100 μg
Destination: France
Envoi sous 6 à 9 jours ouvrables

Aperçu rapide pour SLMAP anticorps (AA 25-607) (ABIN7872886)

Antigène

Voir toutes SLMAP Anticorps
SLMAP (Sarcolemma Associated Protein (SLMAP))

Reactivité

  • 9
  • 3
  • 2
  • 1
Humain, Souris

Hôte

  • 5
  • 4
  • 1
  • 1
Lapin

Clonalité

  • 8
  • 3
Polyclonal

Conjugué

  • 11
Cet anticorp SLMAP est non-conjugé

Application

  • 11
  • 7
  • 3
  • 2
  • 2
  • 1
Western Blotting (WB), ELISA, Flow Cytometry (FACS)
  • Épitope

    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    AA 25-607

    Fonction

    SLMAP Antibody / Sarcolemmal membrane-associated protein

    Purification

    Antigen affinity purified

    Immunogène

    E. coli-derived recombinant human protein (amino acids D25-E607) was used as the immunogen for the SLMAP antibody.

    Isotype

    IgG
  • Indications d'application

    Optimal dilution of the SLMAP 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 SLMAP 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

    SLMAP (Sarcolemma Associated Protein (SLMAP))

    Autre désignation

    SLMAP

    Sujet

    Sarcolemmal membrane-associated protein is a protein that in humans is encoded by the SLMAP gene. This gene encodes a component of a conserved striatin-interacting phosphatase and kinase complex. Striatin family complexes participate in a variety of cellular processes including signaling, cell cycle control, cell migration, Golgi assembly, and apoptosis. The protein encoded by this gene is a coiled-coil, tail-anchored membrane protein with a single C-terminal transmembrane domain that is posttranslationally inserted into membranes. Mutations in this gene are associated with Brugada syndrome, a cardiac channelopathy. Alternative splicing results in multiple transcript variants.

    UniProt

    Q14BN4
Vous êtes ici:
Chat with us!