Tocriscreen Epigenetics 3.0
Biological Activity
Tocriscreen Epigenetics Library is a library of 160 epigenetic compounds (100 μL, 10 mM solutions). Contains compounds covering >40 epigenetic targets including epigenetic readers, writers, erasers and transcriptional modulators. Includes the latest chemical tools to target p300/CBP, PCAF, BRPF1 and SMYD2.This library replaces the Tocriscreen Epigenetics Library (Cat. No. 6801).
If this library does not suit your needs, please submit your requirements through our Tocriscreen PRO custom compound library service.
Key Format and Product Details
- 96-well racks with Matrix storage tubes & SepraSeal caps
- Pre-dissolved in DMSO
- Exceptional purity
- Many compounds are exclusive to Tocris
- Full chemical and biological data available
- Proven solubility, biological activity and stability in DMSO
The Tocriscreen Epigenetics Compound Library contains bioactive compounds covering a diverse range of molecular targets within the following categories: epigenetic writers (43%), transcription modulators (23%), epigenetic erasers (19%), and epigenetic readers (16%).
Request Compound List
A list of the compounds available in the Tocriscreen Epigenetics 3.0 can be requested in Excel or SD format via our Tocriscreen & Custom Library Inquiries form.
Technical Data
The technical data provided above is for guidance only.
For batch specific data refer to the Certificate of Analysis.
Tocris products are intended for laboratory research use only, unless stated otherwise.
Additional Information
Product Datasheets
Citations for Tocriscreen Epigenetics 3.0
The citations listed below are publications that use Tocris products. Selected citations for Tocriscreen Epigenetics 3.0 include:
2 Citations: Showing 1 - 2
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Deciphering a global source of non-genetic heterogeneity in cancer cells.
Authors: Zhang Et al.
Nucleic Acids Res. 2023;51:9019
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Loss of KDM6A activates super-enhancers to induce gender-specific squamous-like pancreatic cancer and confers sensitivity to BET inhibitors.
Authors: Andricovich Et al.
Cancer Cell 2018;33:512
FAQs
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