DTNA anticorps (C-Term)

N° du produit ABIN5516276

Détail du produit anti-DTNA anticorps

Antigène: DTNA (Dystrobrevin alpha (DTNA))

Épitope: C-Term

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp DTNA est non-conjugé

Application: Western Blotting (WB)

Séquence: DMVTEDADPY VQPEDENYEN DSVRQLENEL QMEEYLKQKL QDEAYQVSLQ

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

Purification: Affinity Purified

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

Information d'application

Indications d'application: Optimal working dilution should be determined by the investigator.

Restrictions: For Research Use only

Stockage

Format: Liquid

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

Agent conservateur: Sodium azide

Précaution d'utilisation: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: -20 °C

Stockage commentaire: 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.

Détails sur DTNA

Antigène: DTNA (Dystrobrevin alpha (DTNA))

Autre désignation: DTNA (DTNA Produits)

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

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.

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

ID gène: 1837