DTNA Protein (Transcript Variant 5) (Myc-DYKDDDDK Tag)

Produktnummer ABIN2719789

Produktdetails

Target: DTNA (Dystrobrevin alpha (DTNA))

Protein-Typ: Recombinant

Proteineigenschaft: Transcript Variant 5

Spezies: Human

Quelle: HEK-293 Cells

Aufreinigungstag / Konjugat: Dieses DTNA Protein ist gelabelt mit Myc-DYKDDDDK Tag.

Applikation: Antibody Production (AbP), Standard (STD)

Produktmerkmale:

• Recombinant human DTNA / DRP3 (transcript variant 5) protein expressed in HEK293 cells.
• Produced with end-sequenced ORF clone

Reinheit: > 80 % as determined by SDS-PAGE and Coomassie blue staining

Anwendungsinformationen

Applikationshinweise: Recombinant human proteins can be used for:
Native antigens for optimized antibody production
Positive controls in ELISA and other antibody assays

Kommentare:

The tag is located at the C-terminal.

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Konzentration: 50 μg/mL

Buffer: 25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.

Lagerung: -80 °C

Informationen zur Lagerung: Store at -80°C. Thaw on ice, aliquot to individual single-use tubes, and then re-freeze immediately. Only 2-3 freeze thaw cycles are recommended.

Antigendetails

Target: DTNA (Dystrobrevin alpha (DTNA))

Andere Bezeichnung: Dtna,drp3 (DTNA Produkte)

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

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

NCBI Accession: NP_116761