Histone deacetylases (HDACs) are negative regulators of gene transcription due to their ability to tightly compact heterochromatin by removing acetyl groups from histone tails. Thus, they are considered important targets for anti-cancer therapeutics due to their involvement in cell cycle regulation, cell proliferation, and apoptosis, and overall gene expression. Similarly, the Sirtuin family of deacetylases are targets across a number of therapeutic areas, including cancer, inflammation, and neurodegenerative diseases.
Biochemical Assay Format:
This assay method eliminates dealing with the radioactivity, extraction, and chromatography aspects of other assays. Only two simple steps on a microtiter plate are needed to analyze HDAC activity. First, an HDAC fluorometric substrate is incubated with purified HDAC enzyme. HDAC deacetylation sensitizes the resulting product to subsequent treatment with the developer, which releases a fluorophore that is easily measured on a fluorescence reader. The result is a robust signal that enables sensitive testing of inhibitors.
We offer one of the most extensive suite of HDAC and Sirtuin targets on the market for screening and profiling services. Our team of experts, using our in-house developed biochemical assay kits, can provide:
Screening for inhibitor activity and selectivity across our full panel or just your targets of interest
Determination of IC50
Project guidance and questions answered in a timely manner
Delivery of detailed results promptly and on time
If follow-up studies are required, we can provide the same active proteins as the ones used in our assays.
Available Service Assays
HDAC 1 (Human) (Mouse) | HDAC 6 (Human) (Mouse) | HDAC 9 | SIRT 1 |
| HDAC 2 | HDAC6 (H216A) | HDAC 11 | SIRT 2 |
| HDAC 3 | HDAC6 (H611A) | | SIRT 3 |
| HDAC 4 | HDAC 7 | | SIRT 5 |
| HDAC 5 | HDAC 8 | | SIRT6 |
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