MEOX2 anticorps (C-Term) (Fluoro550)

N° du produit ABIN8009180

Cet anticorps Lapin Polyclonal détecte spécifiquement MEOX2 dans FACS. Il présente une réactivité avec des échantillons de Humain, Rat et Souris.

Aperçu rapide pour MEOX2 anticorps (C-Term) (Fluoro550) (ABIN8009180)

Antigène: MEOX2 (Mesenchyme Homeobox 2 (MEOX2))

Reactivité: Humain, Rat, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp MEOX2 est conjugé à/à la Fluoro550

Application: Flow Cytometry (FACS)

Détail du produit anti-MEOX2 anticorps (Fluoro550)

Épitope: C-Term

Fonction: Anti-MEOX2 Antibody Fluoro550 Conjugated

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

Homologie: Human MEOX2 shares 100% amino acid (aa) sequence identity with both mouse,rat MEOX2.

Purification: Immunogen affinity purified.

Immunogène: A synthetic peptide corresponding to a sequence at the C-terminus of human MEOX2. Human MEOX2 shares 100% amino acid (aa) sequence identity with both mouse and rat MEOX2.

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 MEOX2

Antigène: MEOX2 (Mesenchyme Homeobox 2 (MEOX2))

Autre désignation: MEOX2

Sujet:

Background: This gene encodes a member of a subfamily of non-clustered, diverged, antennapedia-like homeobox-containing genes. The encoded protein may play a role in the regulation of vertebrate limb myogenesis. Mutations in the related mouse protein may be associated with craniofacial and/or skeletal abnormalities, in addition to neurovascular dysfunction observed in Alzheimer's disease.

Gene Full Name: mesenchyme homeobox 2

ID gène: 4223

UniProt: P50222