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EPH Receptor A2 antibody (Biotin)

This anti-EPH Receptor A2 antibody is a Rabbit Monoclonal antibody detecting EPH Receptor A2 in WB, ELISA and FACS. Suitable for Human.
Catalog No. ABIN7608198

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

Target

See all EPH Receptor A2 (EPHA2) Antibodies
EPH Receptor A2 (EPHA2)

Reactivity

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Human

Host

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Rabbit

Clonality

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Monoclonal

Conjugate

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This EPH Receptor A2 antibody is conjugated to Biotin

Application

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

Clone

DM167
  • Purpose

    Biotinylated Anti-EPHA2 antibody(DM167), Rabbit mAb

    Purification

    Purified from cell culture supernatant by affinity chromatography

    Isotype

    IgG
  • Application Notes

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

    Restrictions

    For Research Use only
  • 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

    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
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