TRIM2 anticorps (AA 78-398) (APC)

N° du produit ABIN8049688

Cet anticorps anti-TRIM2 Polyclonal Lapin conjugué à APC (ABIN8049688) détecte spécifiquement TRIM2 dans FACS. L’anticorps est réactif avec des échantillons de Humain, Souris et Rat.

Aperçu rapide pour TRIM2 anticorps (AA 78-398) (APC) (ABIN8049688)

Antigène: TRIM2 (Tripartite Motif Containing 2 (TRIM2))

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp TRIM2 est conjugé à/à la APC

Application: Flow Cytometry (FACS)

Détail du produit anti-TRIM2 anticorps (APC)

Épitope: AA 78-398

Fonction: Anti-TRIM2 Antibody APC Conjugated

Homologie: Human TRIM2 shares 99.4%,98.8% amino acid (aa) sequence identity with mouse,rat TRIM2,respectively.

Purification: Immunogen affinity purified.

Immunogène: E.coli-derived human TRIM2 recombinant protein (Position: Q78-E398). Human TRIM2 shares 99.4% and 98.8% amino acid (aa) sequence identity with mouse and rat TRIM2, respectively.

Isotype: IgG

Information d'application

Indications d'application: Flow Cytometry, Optimal dilutions should be determined by end users.

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: Each vial contains 50 % glycerol, 0.9 % NaCl, 0.2 % Na2HPO4, 0.02 % Sodium azide.

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: At -20°C for one year from date of receipt. Avoid repeated freezing and thawing. Protect from light.

Date de péremption: 12 months

Détails sur TRIM2

Antigène: TRIM2 (Tripartite Motif Containing 2 (TRIM2))

Autre désignation: TRIM2

Sujet:

Background: The protein encoded by this gene is a member of the tripartite motif (TRIM) family. The TRIM motif includes three zinc-binding domains, a RING, a B-box type 1 and a B-box type 2, and a coiled-coil region. The protein localizes to cytoplasmic filaments. It plays a neuroprotective role and functions as an E3-ubiquitin ligase in proteasome-mediated degradation of target proteins. Mutations in this gene can cause early-onset axonal neuropathy. Alternative splicing results in multiple transcript variants.

Gene Full Name: tripartite motif containing 2

ID gène: 23321

UniProt: Q9C040