Myc标签小鼠单克隆抗体(2D5),磁珠偶联

Assay Principle

Anti-Myc Tag Magnetic Beads are prepared by covalently coupling Anti-Myc Tag Mouse Monoclonal Antibody to crosslinked Magnetic Beads, useful for detection and capture of fusion proteins containing a Myc peptide sequence by commonly used immunoprecipitation procedures. The coupling technique is optimized to give a high binding capacity for Myc-Tag protein.

Reagent Required but Not Supplied

Elution Buffer: 0.1 M Glycine-HCl pH 3.0.

Neutralization Buffer: 1 M Tris-HCl, pH 8.5.

Assay Procedure

A. Preparation of magnetic beads

Note: Per 500 μL of protein sample add 20 μL Magnetic Beads. Perform the following procedures, according to add 20 μL Magnetic Beads.

1. Add Magnetic Beads to a 1.5 mL centrifuge tube. Place the centrifuge tube on a Magnetic Separation Rack, let stand for 10 s, remove the supernatant.
2. Add 1 mL 1×TBS to re-suspend Magnetic Beads, place the tube on a Magnetic Separation Rack, let stand for 10 s, remove the supernatant, repeat 3 times. Add 20 μL 1×TBS to re-suspend Magnetic Beads.

B. Immunoprecipitation

1. Add 500 μL protein samples to the processed Magnetic Beads, and incubate at room temperature for 1-2 h or overnight at 4℃ (It is recommended to use vertical rotating mixer with Low-speed rotation).
2. Place the tube on a Magnetic Separation Rack, let stand for 10 s, remove the supernatant.
3. Add 1 mL 1×TBS, and re-suspend Magnetic Beads, place the tube on a Magnetic Separation Rack, let stand for 10 s, remove the supernatant, repeat 3-5 times, until OD280 of the supernatant is lesser than 0.05.
4. Elution
   • a) Denatured elution: This method is suitable for SDS-PAGE and Western Blotting analysis of elution samples. Add 100 μL (5 times volume of Beads) 1×SDS-PAGE Loading Buffer to the tube and mix well, incubate at 100℃ for 5 min, then Centrifuge at 800 rpm for 1 min, and collect the supernatant to a new tube for SDS-PAGE and Western Blotting analysis.
   • b) Competitive elution of peptide: This method can maintain their original biological activity, elution can be used for functional analysis. Add 100 μL (5 times volume of Beads) Myc Peptide (0.1-0.2 μg/mL) to the tube and mix well, incubate at 4℃ for 1-2 h (It is recommended to use vertical rotating mixer with Low-speed rotation), then centrifuge at 800 rpm for 2 min at 4℃, and collect the supernatant which is Myc-Tag protein and its complex to a new tube. In order to improve the elution efficiency, the incubation time can be Increased or repeat elution. Place Myc-Tag protein and its complex on ice to be used, or store at -20℃/-80℃ for long-term. It is recommended to add 100 μL 1×SDS-PAGE Loading Buffer to beads precipitation to test the effect of immunoprecipitation and elution.
   • c) Acid elution: This method can maintain their original biological activity, elution can be used for functional analysis. Add 100 μL (5 times volume of Beads) Elution Buffer to the tube and mix well, incubate at room temperature for 5-10 min (It is recommended to use vertical rotating mixer with Low-speed rotation), then centrifuge at 800 rpm for 2 min at 4℃, and collect the supernatant which is Myc-Tag protein and its complex to a new tube, and immediately add 10 μL Neutralization Buffer to adjust the pH to 7.0-8.0. In order to improve the elution efficiency, elution can be repeated, and combine the same samples. Place His-Tag protein and its complex on ice to be used, or store at -20℃/-80℃ for long-term. It is recommended to add 100 μL 1×SDS-PAGE Loading Buffer to beads precipitation to test the effect of immunoprecipitation and elution.

   Note: a) For a few samples, due to differences in target proteins, the binding of Myc-Tag and Anti-Myc antibody is very strong, and the effect of Acid elution and Competitive elution of peptide may be poor. Therefore, SDS-PAGE Loading Buffer denaturation elution method is recommended as a priority; b) Due to the difference of target protein, the elution efficiency of acid elution method also varies to some extent. If the requirement of elution efficiency is high, the pH value of acidic eluent can be adjusted appropriately between 2.5-3.1, and the pH value or quantity of corresponding neutralizing solution should be adjusted appropriately. For example, 100 μL Acid Elution Buffer (0.1 M Glycine-HCl, pH 2.8) and 15 μL Neutralizing Buffer (1 M Tris-HCl, pH 8.5).

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Disclaimer

The reagent is only used in the field of scientific research, not suitable for clinical diagnosis or other purposes.