DTNA anticorps (C-Term)

N° du produit ABIN951988

Détail du produit anti-DTNA anticorps

Antigène: DTNA (Dystrobrevin alpha (DTNA))

Épitope: AA 691-721, C-Term

Reactivité: Humain, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp DTNA est non-conjugé

Application: Western Blotting (WB), Immunofluorescence (IF), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Enzyme Immunoassay (EIA)

Specificité: This antibody recognizes Human and Mouse DTNA / DRP3 (C-term).

Purification: Affinity Chromatography on Protein A

Immunogène: KLH conjugated synthetic peptide between 691-721 amino acids from the C-terminal region of Human DTNA.

Isotype: Ig Fraction

Information d'application

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

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 0.25 mg/mL

Buffer: PBS with 0.09 % (W/V) Sodium Azide as preservative

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 freezing and thawing.

Stock: 4 °C/-20 °C

Stockage commentaire: Store undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.

Détails sur DTNA

Antigène: DTNA (Dystrobrevin alpha (DTNA))

Autre désignation: DTNA / DRP3 (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.Synonyms: Alpha-dystrobrevin, Dystrobrevin alpha, Dystrophin-related protein 3

Poids moléculaire: 83901 Da

ID gène: 1837

NCBI Accession: NP_001381