DTNA Antikörper

Produktnummer ABIN6292450

Produktdetails anti-DTNA Antikörper

Target: DTNA (Dystrobrevin alpha (DTNA))

Reaktivität: Human, Maus

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser DTNA Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

Aufreinigung: Affinity purification

Immunogen: Recombinant protein of human DTNA

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: WB 1:500 - 1:2000

Kommentare:

Highly expressed in brain, skeletal and cardiac muscles, and expressed at lower levels in lung, liver and pancreas, Isoform 2 is not expressed in cardiac muscle, Isoform 7 and isoform 8 are only expressed in muscle

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Buffer: PBS with 0.02 % sodium azide, 50 % glycerol,  pH 7.3.

Konservierungsmittel: Sodium azide

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

Lagerung: -20 °C

Informationen zur Lagerung: Store at -20C. Avoid freeze / thaw cycles.

Details zu DTNA

Target: DTNA (Dystrobrevin alpha (DTNA))

Andere Bezeichnung: DTNA (DTNA Produkte)

Synonyme: adtn antikoerper, atnb antikoerper, MGC146484 antikoerper, 2210407P21Rik antikoerper, A0 antikoerper, Dtn antikoerper, a-DB-1 antikoerper, adbn antikoerper, D18S892E antikoerper, DRP3 antikoerper, DTN antikoerper, DTN-A antikoerper, LVNC1 antikoerper, Dtna-ps1 antikoerper, RGD1561985 antikoerper, dystrobrevin alpha antikoerper, dystrobrevin, alpha antikoerper, DTNA antikoerper, dtna antikoerper, LOC100195747 antikoerper, Dtna antikoerper

Hintergrund: The protein encoded by this gene belongs to the dystrobrevin subfamily of the dystrophin family. This protein is a component of the dystrophin-associated protein complex (DPC), which consists of dystrophin and several integral and peripheral membrane proteins, including dystroglycans, sarcoglycans, syntrophins and alpha- and beta-dystrobrevin. The DPC localizes to the sarcolemma and its disruption is associated with various forms of muscular dystrophy. Mutations in this gene are associated with left ventricular noncompaction with congenital heart defects. Multiple alternatively spliced transcript variants encoding different isoforms have been identified for this gene.

Molekulargewicht: 83.901 kDa

Gen-ID: 1837

UniProt: Q9Y4J8