DTNA Antikörper (C-Term)

Produktnummer ABIN951988

Dieser Kaninchen Polyklonal Antikörper detektiert spezifisch DTNA in WB, IF, IHC (p) und EIA. Es zeigt Reaktivität gegenüber Proben von Human und Maus.

Kurzübersicht für DTNA Antikörper (C-Term) (ABIN951988)

Target: DTNA (Dystrobrevin alpha (DTNA))

Reaktivität: Human, Maus

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser DTNA Antikörper ist unkonjugiert

Applikation: Western Blotting (WB), Immunofluorescence (IF), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Enzyme Immunoassay (EIA)

Produktdetails anti-DTNA Antikörper

Bindungsspezifität: AA 691-721, C-Term

Spezifität: This antibody recognizes Human and Mouse DTNA / DRP3 (C-term).

Aufreinigung: Affinity Chromatography on Protein A

Immunogen: KLH conjugated synthetic peptide between 691-721 amino acids from the C-terminal region of Human DTNA.

Isotyp: Ig Fraction

Anwendungsinformationen

Applikationshinweise: Optimal working dilution should be determined by the investigator.

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 0.25 mg/mL

Buffer: PBS with 0.09 % (W/V) Sodium Azide as preservative

Konservierungsmittel: Sodium azide

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

Handhabung: Avoid repeated freezing and thawing.

Lagerung: 4 °C/-20 °C

Informationen zur Lagerung: Store undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.

Details zu DTNA

Target: DTNA (Dystrobrevin alpha (DTNA))

Andere Bezeichnung: DTNA / DRP3

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.Synonyms: Alpha-dystrobrevin, Dystrobrevin alpha, Dystrophin-related protein 3

Molekulargewicht: 83901 Da

Gen-ID: 1837

NCBI Accession: NP_001381