Universal Magnetic Co-IP Kit

magnetic beads for low background co-immunoprecipitation

 

Universal Magnetic Co-IP Kit Overview

The Universal Magnetic Co-IP Kit improves co-immunoprecipitation (Co-IP) using protein G-coated magnetic beads, which speed and simplify the procedure while greatly reducing background. The kit includes optimized reagents for making both nuclear & whole cell extracts from cells or tissue, giving you the flexibility to Co-IP any protein complex, whether it was originally bound to DNA or in the cytoplasm.

 

While Co-IP is often used to study cytoplasmic protein complexes, traditional methods are not optimal for studying DNA-binding proteins because these nuclear complexes are fragile and can be difficult to remove from the DNA. This causes them to either be disrupted during extraction, or to be lost because they remain bound to the DNA. For this reason, in addition to containing components for whole-cell extraction, the Universal Magnetic Co-IP Kit provides nuclear extraction reagents that have been optimized to preserve nuclear protein complexes.

Universal Magnetic Co-IP Kit Highlights

  • Flexible: Perform Co-IP of nuclear or cytoplasmic protein complexes, beginning from cells or tissue
  • Gentle: Nuclear extraction procedure removes nuclear protein complexes from the DNA without disrupting protein-protein interactions
  • Fast: Magnetic beads speed and simplify the procedure while reducing background
  • Preserves Proteins: Included inhibitor solutions preserve the integrity of protein modifications
 

Universal Magnetic Co-IP Kit Contents

The Universal Magnetic Co-IP Kit is shipped on dry ice and contains reagents with multiple storage temperatures inside. Please store components according to the storage conditions in the manual after first use. All reagents are guaranteed stable for 6 months from date of receipt when stored properly.

  • 10X PBS, 4°C
  • 10X Hypotonic Buffer, 4°C
  • Whole-cell Lysis Buffer, -20°C
  • Co-IP/Wash Buffer, 4°C
  • Detergent, 4°C
  • 100X Phosphatase Inhibitors, -20°C
  • Protease Inhibitor Cocktail, -20°C
  • Deacetylase Inhibitor, -20°C
  • 100 mM PMSF, -20°C
  • 0.5 M EDTA, 4°C
  • Digestion Buffer, 4°C
  • Enzymatic Shearing Cocktail, -20°C
  • Protein G Magnetic Beads, 4°C
  • Bar Magnet, RT
  • Mini Glue Dots, RT


 

Universal Magnetic Co-IP Kit Data

Co-Immunoprecipitation of a nuclear complex containing SRC-1 and ER alpha from MCF-7 cell nuclear extract using the Universal Magnetic Co-IP Kit

Figure 1: By using magnetic beads, it’s possible to use low stringency buffers while maintaining reduced background.

The Universal Magnetic Co-IP Kit was used to make nuclear extract from MCF-7 cells that had been induced 1 hour with 10 nM Estradiol. IP was performed on 300 µg samples using 2 µg of SRC-1 pAb, ERα pAb and rabbit IgG (as a negative control). Western blot was then performed using the ERα pAb on 10 µg Input Extract, SRC-1 IP, ERα IP and the rabbit IgG IP.


Detection of acetylated Histone H3 in HeLa cell nuclear extract made using the Universal Magnetic Co-IP Kit

Figure 2: Proprietary Enzymatic Shearing Cocktail releases undissociated protein complexes from the DNA so that even histone complexes can be studied.

HeLa nuclear extracts were made using the Universal Magnetic Co-IP Kit or a traditional high-salt extraction protocol, supplemented with 1 µM trichostatin A, a deacetylase inhibitor. Five and ten µg samples of each extract were used in Western Blot with a Histone H3 acetyl pAb. Protein was detected only in samples made using the kit’s nuclear extraction procedure, as it was designed to release histone and other protein complexes from DNA while preserving modifications.

 

Universal Magnetic Co-IP Kit FAQs

What is the difference between the Nuclear Complex Co-IP Kit (Cat No. 54001) and the Universal Magnetic Co-IP Kit (Cat No. 54002)?

Below are the main differences:

Nuclear Complex Co-IP Kit (Cat No. 54001) Universal Magnetic Co-IP kit (Cat No. 54002)
Processes nuclear lysates Processes nuclear and whole-cell lysates
More customizable offering varying stringencies Easier to use
Uses Protein G agarose columns (available separately) Uses magnetic beads (included in kit)

Should I increase the IP stringency when using the Universal Magnetic Co-IP Kit?

The Protein G Magnetic Beads included in the Universal Magnetic Co-IP Kit were chosen because they exhibit a very small degree of non-specific binding. This helps ensure very low background, enabling the Complete Co-IP/Wash Buffer used in the kit to be of low stringency, which better preserves fragile protein complexes. Particular cell lines, stimulations or antibodies may result in higher background. If your experiment has more background than is optimal, we recommend increasing the number of washes performed from 4 to 6.

Is this kit compatible with downstream mass spectrometry (MS/LC-MS)?

Active Motif has not used this kit with downstream mass spectrometry. However, there are many publications where it has been used for this application. Various MS instruments are sensitive to different buffer components. Please consult with your instrument’s manual or core facility to determine any components to avoid and we can let you know if they are present in our buffer systems.

 

 

Universal Magnetic Co-IP Kit Publications

Search our database of customer publications that have used our Universal Magnetic Co-IP Kit.


 
 
 

Universal Magnetic Co-IP Kit Documents

 


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Universal Magnetic Co-IP Kit advantages

  • Perform Co-IP of nuclear or cytoplasmic protein complexes, beginning from cells or tissue
  • Magnetic beads speed and simplify the procedure while reducing background, enabling the use of low-stringency buffers that maintain complex integrity
  • Nuclear extraction procedure removes nuclear protein complexes from the DNA without disrupting protein/protein interactions
  • Inhibitor solutions included to preserve the integrity of protein modifications

Perform Co-IP of cytoplasmic & nuclear protein complexes

While Co-IP is often used to study cytoplasmic protein complexes, traditional methods are not optimal for studying DNA-binding proteins because these nuclear complexes are fragile and can be difficult to remove from the DNA. This causes them to either be disrupted during extraction, or to be lost because they remain bound to the DNA. For this reason, in addition to containing components for whole-cell extraction, the Universal Magnetic Co-IP Kit provides nuclear extraction reagents that have been optimized to preserve nuclear protein complexes. The reduced background provided by the low non-specific binding of the kit's magnetic beads makes it possible to use a low-stringency Co-IP/Wash Buffer that helps maintain the protein complexes (Figure 1). To further improve Co-IP of nuclear complexes, the kit’s proprietary Enzymatic Shearing Cocktail uses DNA digestion to release undissociated protein complexes from the DNA. Even histone complexes, which are not released from the DNA by traditional high-salt extraction methods, can be studied (Figure 2).

Co-Immunoprecipitation of a nuclear complex containing SRC-1 and ER alpha from MCF-7 cell nuclear extract using the Universal Magnetic Co-IP Kit

Figure 1: Co-Immunoprecipitation of a nuclear complex containing SRC-1 and ERα.

The Universal Magnetic Co-IP Kit was used to make nuclear extract from MCF-7 cells that had been induced 1 hour with 10 nM Estradiol. IP was performed on 300 µg samples using 2 µg of SRC-1 pAb, ERα pAb and rabbit IgG (as a negative control). Western blot was then performed using the ERα pAb on 10 µg Input Extract, SRC-1 IP, ERα IP and the rabbit IgG IP.


Detection of acetylated Histone H3 in HeLa cell nuclear extract made using the Universal Magnetic Co-IP Kit

Figure 2: Detection of acetylated Histone H3.

HeLa nuclear extracts were made using the Universal Magnetic Co-IP Kit and a traditional high-salt extraction protocol, supplemented with 1 µM trichostatin A, a deacetylase inhibitor. Five and ten µg samples of each extract were used in Western with Histone H3 acetyl pAb. Protein was detected only in samples made using the kit’s nuclear extraction procedure, as it was designed to release histone and other protein complexes from DNA while preserving modifications.

Contents & Storage

Each Universal Magnetic Co-IP Kit provides sufficient reagents to make 25 nuclear and 25 whole-cell extractions, and then to perform 25 co-immunoprecipitations. Kits include PBS, Hypotonic Buffer, Whole-cell Lysis Buffer, Co-IP/Wash Buffer, Phosphatase Inhibitors, Protease Inhibitor Cocktail, Deacetylase Inhibitor, PMSF, EDTA, Digestion Buffer, Enzymatic Shearing Cocktail, Detergent, Protein G Magnetic Beads and a Bar Magnet for making a magnetic stand. The reagent storage conditions vary from room temperature to -20°C. Please download a manual for complete kit specifications and storage conditions. All reagents are guaranteed stable for 6 months when stored properly.

The following publications cite the use of and/or provide additional information about the Universal Magnetic Co-IP Kit: