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SNTG2 anticorps (AA 100-430)

Cet anticorps Lapin Polyclonal détecte spécifiquement SNTG2 dans WB, ELISA et FACS. Il présente une réactivité avec des échantillons de Humain, Souris et Rat.
N° du produit ABIN7869875
644,88 €
Plus frais de livraison 40,00 € et TVA
100 μg
Destination: France
Envoi sous 6 à 9 jours ouvrables

Aperçu rapide pour SNTG2 anticorps (AA 100-430) (ABIN7869875)

Antigène

Voir toutes SNTG2 Anticorps
SNTG2 (Syntrophin, gamma 2 (SNTG2))

Reactivité

  • 22
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Humain, Souris, Rat

Hôte

  • 21
  • 1
Lapin

Clonalité

  • 22
Polyclonal

Conjugué

  • 8
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp SNTG2 est non-conjugé

Application

  • 21
  • 13
  • 13
  • 7
  • 3
  • 3
  • 1
  • 1
  • 1
Western Blotting (WB), ELISA, Flow Cytometry (FACS)
  • Épitope

    • 15
    • 2
    • 1
    • 1
    • 1
    AA 100-430

    Fonction

    Syntrophin gamma 2 Antibody / SNTG2

    Purification

    Antigen affinity purified

    Immunogène

    E. coli-derived recombinant human protein (amino acids I100-R430) was used as the immunogen for the Syntrophin gamma 2 antibody.

    Isotype

    IgG
  • Indications d'application

    Optimal dilution of the Syntrophin gamma 2 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 Syntrophin gamma 2 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

    SNTG2 (Syntrophin, gamma 2 (SNTG2))

    Autre désignation

    Syntrophin gamma 2

    Sujet

    This gene encodes a protein belonging to the syntrophin family. Syntrophins are cytoplasmic peripheral membrane proteins that bind to components of mechanosenstive sodium channels and the extreme carboxy-terminal domain of dystrophin and dystrophin-related proteins. The PDZ domain of this protein product interacts with a protein component of a mechanosensitive sodium channel that affects channel gating. Absence or reduction of this protein product has been associated with Duchenne muscular dystrophy. There is evidence of alternative splicing yet the full-length nature of these variants has not been described.

    UniProt

    Q9NY99
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