MEOX2 antibody

Catalog No. ABIN2460538

This Rabbit Polyclonal antibody specifically detects MEOX2 in WB and ELISA. It exhibits reactivity toward Human, Rat, Mouse and Dog.

Quick Overview for MEOX2 antibody (ABIN2460538)

Target: MEOX2 (Mesenchyme Homeobox 2 (MEOX2))

Reactivity: Human, Rat, Mouse, Dog

Host: Rabbit

Clonality: Polyclonal

Conjugate: This MEOX2 antibody is un-conjugated

Application: Western Blotting (WB), ELISA

Product Details anti-MEOX2 Antibody

Purification: Antibody is purified by protein A chromatography method.

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

Application Details

Application Notes: 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

Handling

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.

Handling Advice: As with any antibody avoid repeat freeze-thaw cycles.

Storage: 4 °C/-20 °C

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

Target Details for MEOX2

Target: MEOX2 (Mesenchyme Homeobox 2 (MEOX2))

Alternative Name: MEOX2

Background: 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.

Molecular Weight: 33 kDa

Gene ID: 4223

NCBI Accession: NP_005915

UniProt: P50222