SNTG2 Antikörper (AA 181-280) (Biotin)

Produktnummer ABIN1389061

Produktdetails anti-SNTG2 Antikörper (Biotin)

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

Bindungsspezifität: AA 181-280

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser SNTG2 Antikörper ist konjugiert mit Biotin

Applikation: Western Blotting (WB), ELISA, Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Homologie: Human,Mouse,Rat

Aufreinigung: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human SNTG2

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: WB 1:300-5000
IHC-P 1:200-400
IHC-F 1:100-500

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 1 μg/μL

Buffer: Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

Konservierungsmittel: ProClin

Vorsichtsmaßnahmen: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.

Lagerung: -20 °C

Informationen zur Lagerung: Store at -20°C for 12 months.

Haltbarkeit: 12 months

Details zu SNTG2

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

Andere Bezeichnung: SNTG2/Syntrophin 5 (SNTG2 Produkte)

Synonyme: MGC84699 antikoerper, SNTG2 antikoerper, G2SYN antikoerper, SYN5 antikoerper, 2210008K22Rik antikoerper, 9530013L23 antikoerper, BB121248 antikoerper, syntrophin, gamma 2 L homeolog antikoerper, syntrophin gamma 2 antikoerper, syntrophin, gamma 2 antikoerper, sntg2.L antikoerper, SNTG2 antikoerper, Sntg2 antikoerper

Hintergrund:

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.