DTNA Antikörper

Produktnummer ABIN2719780

Produktdetails anti-DTNA Antikörper

Target: DTNA (Dystrobrevin alpha (DTNA))

Reaktivität: Human

Wirt: Maus

Klonalität: Monoklonal

Konjugat: Dieser DTNA Antikörper ist unkonjugiert

Applikation: Western Blotting (WB), Immunofluorescence (IF)

Produktmerkmale: Homo sapiens dystrobrevin, alpha (DTNA), transcript variant 5

Aufreinigung: Purified from mouse ascites fluids by affinity chromatography

Immunogen: Full length human recombinant protein of human DTNA (NP_116761) produced in HEK293T cell.

Klon: 1G1

Isotyp: IgG2b

Anwendungsinformationen

Applikationshinweise: WB 1:500, IF 1:100,

Kommentare:

The concentration of the product may vary between diferrent lots.

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 0.5-1.0 mg/mL

Buffer: PBS (PH 7.3) containing 1 % BSA, 50 % glycerol and 0.02 % sodium azide.

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

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: 58.7 kDa

Gen-ID: 1837

NCBI Accession: NM_032979

HGNC: 1837