Deacetylase Inhibitor Cocktail (100X in 70% DMSO)
- 1. Yan Yan, Xinming Wang, et al. "X-linked ubiquitin-specific peptidase 11 increases tauopathy vulnerability in women." Cell. 2022 Oct 13;185(21):3913-3930.e19. PMID: 36198316
- 2. Yunpeng Wang, Jiaoyu Mao, et al. "lncRNA HOTAIR mediates OGD/R‑induced cell injury and angiogenesis in a EZH2‑dependent manner." Exp Ther Med. 2022 Jan;23(1):99. PMID: 34976141
- 3. Gaojie Song, Jinbo Fang, et al. "Ad-apoptin inhibits glycolysis, migration and invasion in lung cancer cells targeting AMPK/mTOR signaling pathway." Exp Cell Res. 2021 Dec 15;409(2):112926. PMID: 34793774
- 4. Thuy T P Nguyen, Do-Young Kim, et al. "SREBP-1c impairs ULK1 sulfhydration-mediated autophagic flux to promote hepatic steatosis in high-fat-diet-fed mice." Mol Cell. 2021 Sep 16;81(18):3820-3832.e7. PMID: 34233158
Deacetylase Inhibitor Cocktail is a mixture of several chemicals with synergistic functions which is designed to maintain the acetylation state of molecules. Among these targets, dynamic changes of histone acetylation caused by HATs and HDACs are the most often occurring. Lysine acetylation is one of the most important post-translational modification which affects protein transcription, DNA replication and repair, cell cycle, and signal transduction pathways. The balance between acetyltransferases and deacetylases affects chromatin condensation, transcription factor activity and protein aggregation, these modification changes attracts significant interests from researchers. Such, Deacetylation Inhibition Cocktail is a useful tool for assays in these important pathways.
Four components of Deacetylase Inhibitor Cocktail: 40μM Trichostatin A, 1mM EX-527, 400 mM nicotinamide and 200mM sodium butyrate. The compounds are solubilized in 70% DMSO. Each has their own specific capacities. Trichostatin A can inhibit class I/II mammalian HDACs. EX-527 inhibits SIRT1 selectively with less activity on SIRT2 and SIRT3. Nicotinamide could act as an inhibitor of sirtuins (SIRT1-7, Class III HDAC). Sodium Butyrate acts against class I/II HDAC competitively.
Thaw on ice, add at 1:100 (v/v) dilution to solution samples (such as cell lysates or tissue extracts) before assaying.
Applications: WB, Co-IP, pull-down, IF, IHC, Flow Cytometry, kinase assay and etc.
Catalog No. | Product Name | Summary | Targets | CAS Number | Smiles |
A8183 | Trichostatin A (TSA) | HDAC inhibitor | DNA Damage/DNA Repair|HDAC | 58880-19-6 | CC(C=C(C)C=CC(=O)NO)C(=O)C1=CC=C(C=C1)N(C)C |
A4181 | EX 527 (SEN0014196) | SIRT1 inhibitor | Chromatin/Epigenetics|Sirtuin | 49843-98-3 | C1CC(C2=C(C1)C3=C(N2)C=CC(=C3)Cl)C(=O)N |
N1651 | Nicotinamide | PARP-1 inhibitor | Nature Products | 98-92-0 | C1=CC(=CN=C1)C(=O)N |
B1835 | Sodium butyrate | Histone deacetylase inhibitor | 156-54-7 | CCCC(=O)[O-].[Na+] | |
Store at -20°C, and stable for at least 12 months. |