DTNA Protein (Transcript Variant 6) (Myc-DYKDDDDK Tag)

N° du produit ABIN2719787

Détail du produit

Antigène: DTNA (Dystrobrevin alpha (DTNA))

Type de proteíne: Recombinant

Attributs du protein: Transcript Variant 6

Origine: Humain

Source: HEK-293 Cells

Purification/Conjugué: Cette DTNA protéine est marqué à la Myc-DYKDDDDK Tag.

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

Attributs du produit:

• Recombinant human DTNA / DRP3 (transcript variant 6) protein expressed in HEK293 cells.
• Produced with end-sequenced ORF clone

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

Information d'application

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

Commentaires:

The tag is located at the C-terminal.

Restrictions: For Research Use only

Stockage

Concentration: 50 μg/mL

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

Stock: -80 °C

Stockage commentaire: 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.

Détail du antigène

Antigène: DTNA (Dystrobrevin alpha (DTNA))

Autre désignation: Dtna,drp3 (DTNA Produits)

Synonymes: 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

Sujet: 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.

Poids moléculaire: 43.4 kDa

NCBI Accession: NP_116762