SNTG2 Antikörper

Produktnummer ABIN7465582

Der Kaninchen Polyklonal Anti-SNTG2 Antikörper wurde für WB validiert. Er ist geeignet, SNTG2 in Proben von Human zu detektieren.

Kurzübersicht für SNTG2 Antikörper (ABIN7465582)

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

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser SNTG2 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

Produktdetails anti-SNTG2 Antikörper

Kreuzreaktivität: Human

Aufreinigung: Purified by antigen-affinity chromatography.

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

Isotyp: IgG

Anwendungsinformationen

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

Kommentare:

Positive Control: A549 , H1299

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 1 mg/mL

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

Konservierungsmittel: Thimerosal (Merthiolate)

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

Lagerung: 4 °C,-20 °C

Informationen zur Lagerung: 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.

Details zu SNTG2

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

Andere Bezeichnung: syntrophin gamma 2

Hintergrund: 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]

Molekulargewicht: 60 kDa

Gen-ID: 54221

UniProt: Q9NY99