ChIP-IT™ Chromatin Immunoprecipitation Kits

ChIP-IT Kits provide all of the critical components needed for successful ChIP in a single kit. ChIP-IT comes complete with positive & negative control antibodies and PCR primers, DNA purification columns, optimized buffers and a comprehensive manual, all of which have been proven to work in ChIP. For your convenience, kits are available in a variety of formats, with your choice of sonication or our exclusive enzymatic shearing, and either with or without positive & negative controls. This enables you to use the shearing method that works best for you, and to either receive human-specific controls with the kit or to purchase ChIP-IT Control Kits separately to help analyze your results and verify that your antibodies work in the species you choose.

Choose from sonication or reproducible enzymatic shearing

The first step in successful ChIP is shearing the chromatin into 200-1000 bp fragments. This has traditionally been performed using sonication. Although sonication is effective, many users find that complications caused by emulsification and overheating can lead to variable results. To improve reproducibility, Active Motif has developed a unique enzymatic shearing method. For your convenience, all ChIP-IT and ChIP-IT Enzymatic Kits are available in your choice of sonication or enzymatic shearing formats and stand-alone kits are also available. Click here to learn more about your options. And, to make you ChIP even simpler, we also offer Ready-to-ChIP Chromatin. Using our chromatin and ChIP-IT reagents, the only variable in your ChIP will be the antibody you are testing.

Get only the controls you need

ChIP-IT positive and negative controls simplify the task of troubleshooting your experiment, interpreting your results, and validating antibodies for use in ChIP. However, once an antibody has been shown to work in ChIP, it may no longer be necessary to run the controls that are included in the original ChIP-IT Kits. To prevent wasted reagents and unnecessary cost, Active Motif also offers its ChIP-IT Kits without the control reagents. (Likewise, if you are working with a non-human samples, instead of receiving the human controls included in the ChIP-IT Kits, you may want to purchase the ChIP-IT Kit w/o controls together with a ChIP-IT Control Kit for mouse or rat samples.) So, if you already have ChIP-validated antibodies, or if you're working with non-human samples, you can get exactly what you want, without having to pay for controls that you may not need. In addition, Active Motif offers an ever-increasing number of ChIP-validated antibodies, which are ideal for use with ChIP-IT.

Chromatin immunoprecipitation (ChIP) involves the immunoprecipitation of protein/DNA complexes that have been stabilized via cross-linking. It offers a versatile solution by combining the specificity of immunoprecipitation, the sensitivity of PCR and the screening power of array profiling. However, ChIP can be technically challenging and difficult to validate without well-proven reagents. By providing proven antibodies, reagents and controls, ChIP-IT Kits guarantee the best results possible.

Figure 1: Schematic of chromatin immunoprecipitation using ChIP-IT Express.

In ChIP, intact cells are fixed using formaldehyde, which cross-links and therefore preserves protein/DNA interactions. DNA is then sheared into small uniform fragments and the DNA/protein complexes are immunoprecipitated using an antibody directed against the DNA-binding protein of interest. Following immunoprecipitation, the DNA is washed, cross-linking is reversed, and the proteins are removed by Proteinase K treatment. In the original ChIP-IT Kits, the DNA is then rapidly cleaned up using the included DNA purification columns. This DNA purification step in not necessary with ChIP-IT Express (Figure 1). The DNA is then screened to determine which genes were bound by the protein of interest.

Why use ChIP-IT™ Kits?

• Complete solution – all critical reagents needed are supplied
• Direct measurement of protein/DNA interactions, not just histone modifications
• Compatible with genome-wide profiling or selective PCR-based approaches
• No need to optimize reagents and protocol
• No phenol/chloroform extractions – DNA purification columns included in original ChIP-IT Kits, DNA purification step eliminated in ChIP-IT Express

Classically, ChIP has been performed with antibodies directed against abundant chromatin components, such as acetylated histones. While this yields information about transcriptional activity of promoters, it does not reveal which transcription factor is bound to the promoter(s) of interest. In contrast, ChIP using transcription factor-specific antibodies enables direct monitoring of transcription factor/DNA interactions. Unfortunately, this is technically more challenging than classical ChIP, and requires the preparation of several complicated buffers, inhibitor cocktails and blocking reagents. In addition, result validation is difficult without antibodies, controls and a protocol proven to work in ChIP. To overcome these problems and enable ChIP of both transcription factors and histones, Active Motif's ChIP-IT Kits offer a complete solution by providing nearly everything needed to successfully perform ChIP experiments, including positive and negative controls (Figure 2).

Figure 2: Improved chromatin immunoprecipitation using ChIP-IT Express.

A PCR analysis of immunoprecipitated DNA is shown. This figure was selected to demonstrate the efficiency of the ChIP-IT Express Kit. Typically ChIP requires 2 million cells per reaction. However, we have been able to reduce the amount of starting material and observed positive ChIP data from 100,000 cells or less.

HeLa cells were fixed for 10 minutes with 1% formaldehyde and then chromatin was prepared by sonication shearing (5 pulses). ChIP was performed in duplicate on chromatin isolated from 100,000 and 750,000 cells using a Negative Control IgG and an RNA pol II antibody. The DNA isolated through these ChIP reactions was then analyzed by 36 cycles of PCR using GAPDH positive control primers. (These antibodies and primers are available as the ChIP-IT Control Kit – Human. Kits for mouse and rat are also available.) Ten µl of each PCR was separated on a 1% agarose gel and visualized by UV-illumination following ethidium bromide staining. PCR using the GAPDH primers on DNA isolated with the RNA pol II antibody reproducibly generated more product than similar reactions performed on DNA isolated using the Negative Control IgG.These results demonstrate that ChIP performed with RNA pol II antibody greatly enriched for GAPDH promoter DNA, while ChIP performed with negative IgG did not.

Flexible ordering options

The ChIP-IT and ChIP-IT Enzymatic Kits (both with and without controls) include Salmon Sperm DNA/Protein G agarose and the shearing components found in the ChIP-IT Shearing or Enzymatic Shearing Kits, respectively. However, depending on how many immunoprecipitations you perform with each sample of sheared chromatin, you may run out of shearing components before using up all of the immunoprecipitation components in the ChIP-IT Kits. For this reason, the ChIP-IT Sonication & Enzymatic Shearing Kits and the Protein G Magnetic & Agarose Beads are also sold separately.

ChIP-IT Kits provide sufficient components to perform 25 ChIP reactions, and sufficient shearing components to optimize shearing conditions and then make 5 preparations of sheared chromatin from three 15 cm plates (4.5 x 10⁷ cells); each chromatin preparation will yield enough material to perform approximately 16 ChIP reactions. Kits that contain controls include sufficient positive & negative control antibodies and human-specific PCR primer sets to perform 5 control ChIP reactions each.

Contents & Storage

Pre-blocked Protein G agarose, Shearing Buffer (or Digestion Buffer and Enzymatic Shearing Cocktail), ChIP Antibody Binding, DNA Binding, Wash and 10X PCR Buffers, 10X PBS, 10X Glycine, 1X Lysis Buffer, Protease Inhibitor Cocktail, PMSF, EDTA, Proteinase K, RNase A, DNA purification columns and buffers, and Positive Control antibody, Negative Control IgG, and human-specific positive & negative control PCR primer sets. 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.