DTNA Antikörper (C-Term)

Produktnummer ABIN2788807

Dieses Anti-DTNA-Antikörper ist ein Kaninchen Polyklonal-Antikörper zur Detektion von DTNA in WB. Geeignet für Human, Maus, Ratte, Hund, Pferd, Rind (Kuh), Meerschweinchen und Saccharomyces cerevisiae.

Kurzübersicht für DTNA Antikörper (C-Term) (ABIN2788807)

Target: DTNA (Dystrobrevin alpha (DTNA))

Reaktivität: Human, Maus, Ratte, Hund, Pferd, Rind (Kuh), Meerschweinchen, Saccharomyces cerevisiae

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser DTNA Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

Produktdetails anti-DTNA Antikörper

Bindungsspezifität: C-Term

Sequenz: GATTSTMRGD MVTEDADPYV QPEDENYEND SVRQLENELQ MEEYLKQKLQ

Homologie: Cow: 92%, Dog: 100%, Guinea Pig: 93%, Horse: 100%, Human: 100%, Mouse: 86%, Rat: 92%, Yeast: 83%

Produktmerkmale: This is a rabbit polyclonal antibody against DTNA. It was validated on Western Blot.

Aufreinigung: Affinity Purified

Anwendungsinformationen

Applikationshinweise: Optimal working dilutions should be determined experimentally by the investigator.

Kommentare:

Antigen size: 452 AA

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: Lot specific

Buffer: Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.

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 freeze-thaw cycles.

Lagerung: -20 °C

Informationen zur Lagerung: For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.

Details zu DTNA

Target: DTNA (Dystrobrevin alpha (DTNA))

Andere Bezeichnung: DTNA

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.
Alias Symbols: D18S892E, DRP3, DTN, FLJ96209, LVNC1
Protein Interaction Partner: SNTA1, ADRA1D, TJP1, ACTB, MLC1, NUP62, SEC23A, SEC24C, PSEN1, MYO1E, GFI1B, MARK2, SYNC, SNTG2, SNTG1, KCNJ12, SYNM, DTNBP1, SNTB2, SNTB1, DMD, DRP2, UTRN, ACTA1,
Protein Size: 452

Molekulargewicht: 49 kDa

Gen-ID: 1837

NCBI Accession: NM_001198942, NP_001185871

UniProt: B4DIR0