RARS2 anticorps (AA 1-560) (Fluoro647)

N° du produit ABIN7970102

Cet anticorps anti-RARS2 Polyclonal Lapin conjugué à Fluoro647 (ABIN7970102) détecte spécifiquement RARS2 dans FACS. L’anticorps est réactif avec des échantillons de Humain, Souris et Rat.

Aperçu rapide pour RARS2 anticorps (AA 1-560) (Fluoro647) (ABIN7970102)

Antigène: RARS2 (Arginyl-tRNA Synthetase 2, Mitochondrial (RARS2))

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp RARS2 est conjugé à/à la Fluoro647

Application: Flow Cytometry (FACS)

Détail du produit anti-RARS2 anticorps (Fluoro647)

Épitope: AA 1-560

Fonction: Anti-RARS2 Antibody Fluoro647 Conjugated

Réactivité croisée (Details): No cross-reactivity with other proteins

Homologie: Human RARS2 shares 86.1% amino acid (aa) sequence identity with mouse RARS2.

Purification: Immunogen affinity purified.

Immunogène: E.coli-derived human RARS2 recombinant protein (Position: M1-R560). Human RARS2 shares 86.1% amino acid (aa) sequence identity with mouse RARS2.

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 RARS2

Antigène: RARS2 (Arginyl-tRNA Synthetase 2, Mitochondrial (RARS2))

Autre désignation: RARS2

Sujet:

Background: This nuclear gene encodes a protein that localizes to the mitochondria, where it catalyzes the transfer of L-arginine to its cognate tRNA, an important step in translation of mitochondrially-encoded proteins. Defects in this gene are a cause of pontocerebellar hypoplasia type 6 (PCH6). Alternative splicing results in multiple transcript variants.

Gene Full Name: arginyl-tRNA synthetase 2, mitochondrial

ID gène: 57038

UniProt: Q5T160