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HDAC Activity Colorimetric Assay Kit

based on 36 citations in multiple journalsHDAC Activity Colorimetric Assay Kit365 5
Two step assay, HTS
Catalog #: K331

In stock


Product Details

Cat # +Size K331-100
Size 100 assays
Detection Method Absorbance (400 or 405 nm)
Species Reactivity Mammalian
Applications Well suited for high throughput applications. HDAC inhibitors and substrates and related antibodies are also available separately.
Features & Benefits • Simple two-step procedure; takes around than 1 hour
• Fast and convenient
• The assay method eliminates radioactivity/extractions/ and/or chromatography as used in the traditional assays.
Kit Components • HDAC Substrate [Ac-Lys(Ac)-pNA, 10 mM]
• 10X HDAC Assay Buffer
• Lysine Developer
• HDAC Inhibitor (Trichostatin A, 1 mM)
• HeLa Nuclear Extract (5 mg/ml)
• Deacetylated Standard (Ac-Lys-pNA, 10 mM)
Storage Conditions -80°C
Shipping Conditions Dry Ice
USAGE For Research Use Only! Not For Use in Humans.


Inhibition of histone deacetylases (HDACs) has been implicated to modulate transcription and to induce apoptosis or differentiation in cancer cells. However, screening HDAC inhibitory compounds has proven to be difficult over the past due to the lack of convenient tools for analyzing HDAC activity. The new Colorimetric HDAC Activity Assay Kit provides a fast and convenient colorimetric method that eliminates radioactivity, extractions, or chromatography, as used in the traditional assays. The new method requires only two easy steps, both performed on the same microtiter plate. First, the HDAC colorimetric substrate, which comprises an acetylated lysine side chain, is incubated with a sample containing HDAC activity (e.g., HeLa nuclear extract or your own samples). Deacetylation of the substrate sensitizes the substrate, so that, in the second step, trea™ent with the Lysine Developer produces a chromophore. The chromophore can be easily analyzed using an ELISA plate reader or spectrophotometer. The assay is well suited for high throughput screening applications. HDAC inhibitors and antibodies are also available separately.

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Which HDAC kits among K330 and K331 is more sensitive?
K330-100 the Fluorometric Assay Kit is more sensitive (~5 times more sensitive than K331-100 the Colorimetric Assay Kit).
Which HDACs these assays detect?
The assays detect eventually all HDACs that can deacetylate histone.
DTT & Protease Inhibitor Interfere with the assay?
DTT or regular low dose of protease inhibitors should not interfere with the assay. High dose protease inhibitor may interfere the developer.
Which assays are more sensitive: Radioactive methods or your kits?
Radioactive detections are rather too complicated and involves in radioactive materials which are difficult to handle. We have not done direct comparison studies with the radioactive methods.
Can we use frozen tissues?
Yes, you can use frozen tissue. If you keep the tissue in -80C,it can stable for years (do not let the tissue dry. You need 10 to 20 mg of tissue to make lysate. The fluorometric assay is a little more sensitive (~4 FOLD) if you have a flourescence reader.
Can we run this experiment in a 1.5 ml cuvette?
Yes, but you need to scale up the quantities by 5 folds.
What are the sensitivities of the HDAC substrates?
Here are the sensitivities for our HDAC kits K330 and K331: K330-100 (Fluorometric): 0.5 - 10 µg of nuclear extract. K331-100 (Colorimetric): 10 – 200 µg of nuclear extract
Can this kit be used with samples like bacteria, plants, drosophila, yeast etc?
We have optimized the kit with mammalian samples. However, theoretically these kits should work with samples from multiple species/sources. Since the optimal conditions depend on the sample type, the protocol has to be be adapted to fit the samples for efficient results. Please refer to this kit's citations to see what kind of samples have been used with this kit other than mammalian samples.
Can we use frozen samples with this assay?
Fresh samples are always preferred over frozen samples. However, frozen samples can also be used, provided, they were frozen right after isolation, were not freeze thawed multiple time (for which we recommend aliquoting the samples before freezing) and have been frozen for relatively short periods.
Can we use a different wavelength than recommended for the final analysis?
It is always recommended to use the exact recommended wavelength for the most efficient results. However, most plate readers have flexibility in their band width of detection in increments of +/- 10 nm. Depending on this flexibility range, you can deviate from the recommended wavelengths within limits.
What is the exact volume of sample required for this assay?
There is no specific volume we can recommend for the amount any sample to be used since it is completely sample concentration and quality based. You have to do a pilot expt with multiple sample volumes to determine the optimal volume which gives a reading within the linear range of the standard curve. Please refer to the citations for this product to see what other clients have used with similar sample types.
Do you have trial sizes of this kit?
Unfortunately, we do not have trial sizes of this kit available. However, if you are based in the US or Canada, we will give you a 10% off list price introductory discount on its purchase price. If you are based out of this area please contact your regional BioVision distributor.
What is the shelf life of this kit?
This kit is good for 12 months from the date of shipment in the unopened form when stored at the appropriate temperature and appropriate conditions. After opening and reconstitution, some of the components in this kit are good for 2 months at -20°C. Please refer to the datasheet for storage information and shelf life of each of the components.
Why are my standard curve values lower than those shown on the datasheet?
There are multiple factors which influence the signals like the incubation times, room temperature, handling etc. In general, to increase the value of the standards, you can increase the incubation time. As long as the standard curve is linear, it should be fine to use, since all of your samples will also be measured under the same conditions on this curve.
How do I normalize my samples against protein concentration
You can use a protein quantitation assay on the supernatants you get from cell/tissue lysates or with any other liquid sample in the assay buffer.
Can we purchase individual components of this kit?
Yes, you can purchase any of the kit's components without the whole kit. Please refer to the component Cat #s mentioned on the datasheet for ordering.
Can we use an alternate buffer for sample preparation (cell lysis, sample dilutions etc)?
Our assay buffers are optimized for the reactions they are designed for. They not only contain some detergents for efficient lysis of your cells/tissue, but also contain some proprietary components required for the further reactions. Therefore, we highly recommend using the buffers provided in the kit for the best results.
Should I make a standard curve for every expt I do, or is one curve/kit enough?
Yes, I would strongly recommend you to do the standards every time you do the expt. There is always a chance that something was done differently that day and we do not want any conditions to differ between standards and samples.
Tzeng, Haiyue et al. (2016) Antioxidant-Rich Extract from Plantaginis Semen Ameliorates Diabetic Retinal Injury in a Streptozotocin-Induced Diabetic Rat Model, Nutrients. 2016 Sep 18;8(9).
Gurav et al., Slc5a8, a Na+-coupled high-affinity transporter for short-chain fatty acids, is a conditional tumour suppressor in colon that protects against colitis and colon cancer under low-fibre dietary conditions. Biochem. J., Jul 2015; 469: 267 - 278.
Yang et al., PARP-1 Mediates LPS-Induced HMGB1 Release by Macrophages through Regulation of HMGB1 Acetylation.J. Immunol., Dec 2014; 193: 6114 - 6123.
Zhang et al., Specific inhibition of HDAC4 in cardiac progenitor cells enhances myocardial repairs. Am J Physiol Cell Physiol, Aug 2014; 307: C358 - C372.
Aslan et al., Histone deacetylase 6-mediated deacetylation of α-tubulin coordinates cytoskeletal and signaling events during platelet activation. Am J Physiol Cell Physiol, Dec 2013; 305: C1230 - C1239.
For more citations of this product click here
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