SNTG2 anticorps

N° du produit ABIN7465582

L’anticorps anti-SNTG2 Polyclonal Lapin est utilisé pour la détection de SNTG2 dans des échantillons de Humain. Il a été validé pour WB.

Aperçu rapide pour SNTG2 anticorps (ABIN7465582)

Antigène: SNTG2 (Syntrophin, gamma 2 (SNTG2))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp SNTG2 est non-conjugé

Application: Western Blotting (WB)

Détail du produit anti-SNTG2 anticorps

Réactivité croisée: Humain

Purification: Purified by antigen-affinity chromatography.

Immunogène: Recombinant protein encompassing a sequence within the center region of human Syntrophin gamma 2. The exact sequence is proprietary.

Isotype: IgG

Information d'application

Indications d'application: WB: 1:500-1:3000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.

Commentaires:

Positive Control: A549 , H1299

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

Buffer: 1XPBS ( pH 7), 20 % Glycerol, 0.01 % Thimerosal

Agent conservateur: Thimerosal (Merthiolate)

Précaution d'utilisation: This product contains Thimerosal (Merthiolate): a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: 4 °C,-20 °C

Stockage commentaire: Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.

Détails sur SNTG2

Antigène: SNTG2 (Syntrophin, gamma 2 (SNTG2))

Autre désignation: syntrophin gamma 2

Sujet: Syntrophin gamma 2 , G2SYN , SYN5,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. [provided by RefSeq, Jul 2008]

Poids moléculaire: 60 kDa

ID gène: 54221

UniProt: Q9NY99