Anti-Myc magnetic beads

For research use only.

Anti-Myc magnetic beads kit is based on hydroxyl magnetic beads covalently coupling with high quality mouse IgG1 monoclonal antibody.

Anti-Myc magnetic beads

Selleck's has been cited by 41 publications

Advantages

Time saving: save 15-30 min comparing with agarose beads.

Simple operation: Magnetic separation and centrifugation-free.

High protein loading capacity.

High specificity.

Price Comparison

Description

Anti-Myc magnetic beads kit is based on hydroxyl magnetic beads covalently coupling with high quality mouse IgG1 monoclonal antibody. With high loading of Myc-tagged protein (more than 0.6 mg protein/mL) and high specificity, it is recommended to use for co-immunoprecipitation and protein purification.

Properties

Antibody isotype Mouse IgG1
Antibody purification Protein A purified
Application Immunoprecipitation and protein Purification
Recommended volume IP: 20 μL beads for 200 μL crude protein solution
Binding capacity Minimum 0.6 mg protein eluted per ml of magnetic beads

Storage (From the date of receipt)

Store at 2-8°C for 2 years. DO NOT freeze or centrifuge Magnetic Beads.

Protocol

Trouble Shooting

Problem Possible Reason Suggested Improvement
High background Nonspecifically binding of proteins to the antibody, megnetic beads or EP tubes Pre-clear lysate to remove nonspecific binding proteins.
After suspending beads for the final wash, transfer the entire sample to a clean EP tube and then centrifugation.
Washing times are not sufficient. Increase the number of washes.
Increase duration time of washes.
No signal is observed. Myc tagged protein is not expressed in the sample. Make sure the protein of interest contains the Myc sequence.
Prepare the fresh lysate.
Use appropriate protease inhibitors.
Incubation times are inadequate. Increase the incubation times.
Interfering substance is present in sample. The lysate may contain high concentrations of dithiothreitol (DTT), 2-mercaptoethanol, or other reducing agents.
Excessive detergent concentration may interfere with the antibody-antigen interaction.

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