DTNA anticorps (C-Term)

N° du produit ABIN2788807

Cet anticorps anti-DTNA est un anticorps Lapin Polyclonal détectant DTNA dans WB. Adapté pour Humain, Souris, Rat, Chien, Cheval, Boeuf (Vache), Cobaye et Saccharomyces cerevisiae.

Aperçu rapide pour DTNA anticorps (C-Term) (ABIN2788807)

Antigène: DTNA (Dystrobrevin alpha (DTNA))

Reactivité: Humain, Souris, Rat, Chien, Cheval, Boeuf (Vache), Cobaye, Saccharomyces cerevisiae

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp DTNA est non-conjugé

Application: Western Blotting (WB)

Détail du produit anti-DTNA anticorps

Épitope: C-Term

Séquence: GATTSTMRGD MVTEDADPYV QPEDENYEND SVRQLENELQ MEEYLKQKLQ

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

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

Purification: Affinity Purified

Information d'application

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

Commentaires:

Antigen size: 452 AA

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: Lot specific

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.

Conseil sur la manipulation: Avoid repeated freeze-thaw cycles.

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

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: 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

Poids moléculaire: 49 kDa

ID gène: 1837

NCBI Accession: NM_001198942, NP_001185871

UniProt: B4DIR0