SNTG2 anticorps (AA 181-280)

N° du produit ABIN1385151

Cet anticorps anti-SNTG2 Polyclonal Lapin (ABIN1385151) détecte spécifiquement SNTG2 dans WB, IF (cc), IF (p), IHC (fro) et IHC (p). L’anticorps est réactif avec des échantillons de Humain.

Aperçu rapide pour SNTG2 anticorps (AA 181-280) (ABIN1385151)

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

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp SNTG2 est non-conjugé

Application: Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Détail du produit anti-SNTG2 anticorps

Épitope: AA 181-280

Fonction: SNTG2 Polyclonal Antibody

Homologie: Human,Mouse,Rat

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human SNTG2

Isotype: IgG

Information d'application

Indications d'application: WB(1:300-5000),

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 μg/μL

Buffer: 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.

Agent conservateur: ProClin

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

Stock: 4 °C,-20 °C

Stockage commentaire: Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.

Date de péremption: 12 months

Détails sur SNTG2

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

Autre désignation: SNTG2/Syntrophin 5

Sujet:

Synonyms: G2SYN, Gamma2-syntrophin, SNTG2, SYN5, Syntrophin-5, Syntrophin5, Syntrophin 5, Syntrophin gamma 2, SNTG2_HUMAN.

Background: 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.