MEOX2 anticorps

N° du produit ABIN2460538

Cet anticorps Lapin Polyclonal détecte spécifiquement MEOX2 dans WB et ELISA. Il présente une réactivité envers Humain, Rat, Souris et Chien.

Aperçu rapide pour MEOX2 anticorps (ABIN2460538)

Antigène: MEOX2 (Mesenchyme Homeobox 2 (MEOX2))

Reactivité: Humain, Rat, Souris, Chien

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp MEOX2 est non-conjugé

Application: Western Blotting (WB), ELISA

Détail du produit anti-MEOX2 anticorps

Purification: Antibody is purified by protein A chromatography method.

Immunogène: Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human MEOX2.

Information d'application

Indications d'application: MEOX2 antibody can be used for detection of MEOX2 by ELISA at 1:312500. MEOX2 antibody can be used for detection of MEOX2 by western blot at 2.5 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.

Restrictions: For Research Use only

Stockage

Format: Lyophilized

Reconstitution: Add 100 ?L of distilled water. Final antibody concentration is 1 mg/mL.

Concentration: 1 mg/mL

Buffer: Antibody is lyophilized in PBS buffer with 2 % sucrose.

Conseil sur la manipulation: As with any antibody avoid repeat freeze-thaw cycles.

Stock: 4 °C/-20 °C

Stockage commentaire: For short periods of storage (days) store at 4 °C. For longer periods of storage, store MEOX2 antibody at -20 °C.

Détails sur MEOX2

Antigène: MEOX2 (Mesenchyme Homeobox 2 (MEOX2))

Autre désignation: MEOX2

Sujet: MEOX2 is a member of a subfamily of non-clustered, diverged, antennapedia-like homeobox-containing genes. MEOX2 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.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.

Poids moléculaire: 33 kDa

ID gène: 4223

NCBI Accession: NP_005915

UniProt: P50222