EPH Receptor A2 antibody (Biotin)

Catalog No. ABIN7608198

The Biotin-conjugated Rabbit Monoclonal anti-EPH Receptor A2 antibody (Clone DM167) (ABIN7608198) specifically detects EPH Receptor A2 in WB, ELISA and FACS. The antibody is reactive with Human samples.

Quick Overview for EPH Receptor A2 antibody (Biotin) (ABIN7608198)

Target: EPH Receptor A2 (EPHA2)

Reactivity: Human

Host: Rabbit

Clonality: Monoclonal

Conjugate: This EPH Receptor A2 antibody is conjugated to Biotin

Application: Western Blotting (WB), ELISA, Flow Cytometry (FACS)

Clone: DM167

Product Details anti-EPH Receptor A2 Antibody (Biotin)

Purpose: Biotinylated Anti-EPHA2 antibody(DM167), Rabbit mAb

Purification: Purified from cell culture supernatant by affinity chromatography

Isotype: IgG

Application Details

Application Notes: ELISA 1:5000-10000, Flow Cyt 1:100, WB 1:1000

Restrictions: For Research Use only

Handling

Format: Lyophilized

Buffer: Lyophilized from sterile PBS, pH 7.4. Normally 5 % - 8 % trehalose is added as protectants before lyophilization.

Storage: -20 °C,-80 °C

Storage Comment: Store at -20°C to -80°C for 12 months in lyophilized form. After reconstitution, if not intended for use within a month, aliquot and store at -80°C (Avoid repeated freezing and thawing). Lyophilized proteins are shipped at ambient temperature.

Expiry Date: 12 months

Target Details for EPH Receptor A2

Target: EPH Receptor A2 (EPHA2)

Alternative Name: EPHA2

Background: This gene belongs to the ephrin receptor subfamily of the protein-tyrosine kinase family. EPH and EPH-related receptors have been implicated in mediating developmental events, particularly in the nervous system. Receptors in the EPH subfamily typically have a single kinase domain and an extracellular region containing a Cys-rich domain and 2 fibronectin type III repeats. The ephrin receptors are divided into 2 groups based on the similarity of their extracellular domain sequences and their affinities for binding ephrin-A and ephrin-B ligands. This gene encodes a protein that binds ephrin-A ligands. Mutations in this gene are the cause of certain genetically-related cataract disorders.

UniProt: P29317

Pathways: RTK Signaling