DTNA Antikörper (C-Term)

Produktnummer ABIN5516276

Produktdetails anti-DTNA Antikörper

Target: DTNA (Dystrobrevin alpha (DTNA))

Bindungsspezifität: C-Term

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser DTNA Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

Sequenz: DMVTEDADPY VQPEDENYEN DSVRQLENEL QMEEYLKQKL QDEAYQVSLQ

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

Aufreinigung: Affinity Purified

Immunogen: The immunogen is a synthetic peptide directed towards the C-terminal region of Human DTNA

Anwendungsinformationen

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

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

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.

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 (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.

Alias Symbols: DTNA, DRP3,

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: 391

Gen-ID: 1837