CST BLOG: Lab Expectations

The official blog of Cell Signaling Technology (CST), where we discuss what to expect from your time at the bench, share tips, tricks, and information.

Tech Tips Video: How much antibody should I use for ChIP?

Read More
All Posts

It's time to check out another video from the CST Tech Tips playlist! In this edition of Tech Tips, we'll tackle a common protocol question customers ask our ChIP team: how much antibody to use for chromatin immunoprecipitation (ChIP) experiments? Adding more antibody isn't always better - watch the video to learn why. 

Can't see the embedded video above? Click the link below to play: 

How much antibody should I use in ChIP assays? | CST Tech Tips
 

Don't forget to subscribe to CST's YouTube channel for more videos to help your research!

 Subscribe

Transcript:

How much antibody should I use in a ChIP assay? I'm Fang Chen, Senior Scientist in the ChIP group at Cell Signaling Technology, and this is CST Tech Tips.

The optimal amount of antibody to use in a ChIP assay varies, depending on the antibody's affinity, sensitivity and specificity. More antibody is not always better.

As you can see in this titration data, both too much and too little antibody decreases ChIP signal. For most ChIP-validated antibodies, 0.5-2 µg of antibody generates an optimal signal-to-noise ratio in the ChIP assay.

18-CHP26237-data
During our in-house antibody validation efforts, scientists on the ChIP team perform titration experiments using 10 µg of chromatin per IP in order to identify the optimal antibody dilution and then provide that information to you.

It's very important to maintain the ratio of antibody volume to the amount of the chromatin, rather than the ratio of antibody volume to the IP volume. For example, CST recommends using 10 µg of chromatin DNA per IP. However, if less than 10 µg of chromatin DNA is used, then the antibody amount should be decreased proportionally.

CST recommends a total volume of 500 µL for each IP. If ChIP is performed with same amount of DNA but in a larger IP volume, then no extra antibody is required, although a longer incubation time might be helpful to compensate for the diluted reaction.

For a control antibody such as IgG, you should use an equivalent amount as your test antibody for a fair comparison.

Thank you for watching. You can find the full protocol course for all applications on each antibody's product page at cellsignal.com.

If you have any questions about an antibody or protocol, you can get in touch with one of our scientists at cellsignal.com/support.

Don't forget to subscribe for your new Tech Tips videos, and we will see you next time.

Good luck with your experiments!

Kenneth Buck, PhD
Kenneth Buck, PhD
A cell biologist by training, Ken received a PhD at Rutgers and continued as a postdoctoral fellow at Yale, where he studied cytoskeletal dynamics and signaling mechanisms involved in the cellular motility of regenerating neurons. At CST, Ken collaborates with scientists to create multimedia scientific communications. When he's not writing video scripts or in the studio, he can be observed in his natural habitat, mountain biking with colleagues on the rocky North Shore of Massachusetts.

Recent Posts

Cell Preparation Tips for Accurate Flow Cytometry Data

Generating accurate flow cytometry data requires more than just specific and sensitive antibodies validat...
Andrea Tu, PhD Nov 6, 2024

500 Antibodies & Counting: Accelerating Discovery with CST Antibodies Validated for Simple Western Technology

Since 2022, Cell Signaling Technology (CST) and Bio-Techne have been working together to bring best-in-cl...
Chris LaBreck, PhD Oct 23, 2024

Menin-KMT2A Inhibitors: A Promising Approach to Acute Myeloid Leukemia (AML) Treatment

Accounting for about 80% of adult acute leukemias, acute myeloid leukemia (AML) is an aggressive form of ...
Homa Rahnamoun, PhD Oct 16, 2024