EHZF inhibitors are a class of chemical compounds that specifically target and inhibit the activity of the enhancer of zeste homolog (EZH), a protein that plays a crucial role in gene regulation through chromatin modification. EHZF, often referred to in the context of EHZF-like proteins, is involved in the regulation of gene expression by modulating the structure of chromatin, making certain regions of the DNA more or less accessible for transcription. This modulation is critical for various cellular processes, including differentiation, development, and the maintenance of cellular identity. EHZF inhibitors interfere with these processes by blocking the enzymatic activity of EHZF proteins, thereby preventing the addition of methyl groups to histone proteins, a key mechanism by which these proteins exert their regulatory functions.
Inhibitors of EHZF are valuable tools in research aimed at understanding the complex dynamics of epigenetic regulation. By selectively inhibiting EHZF activity, researchers can study the specific roles that these proteins play in chromatin remodeling and gene expression. This can help uncover how changes in chromatin structure influence cellular behavior and contribute to the regulation of various biological processes. Additionally, EHZF inhibitors can be used to explore the broader network of interactions within the cell that are influenced by chromatin state, providing insights into how epigenetic modifications are coordinated and maintained. These inhibitors are particularly useful in experiments designed to probe the mechanisms underlying gene silencing and activation, as well as in studies focused on the long-term stability of gene expression patterns across different cell types and developmental stages. Overall, EHZF inhibitors are powerful tools for advancing our understanding of epigenetics and the intricate molecular mechanisms that regulate gene expression in eukaryotic cells.
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产品名称 | CAS # | 产品编号 | 数量 | 价格 | 应用 | 排名 |
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Bicalutamide | 90357-06-5 | sc-202976 sc-202976A | 100 mg 500 mg | $41.00 $143.00 | 27 | |
这种雄激素受体拮抗剂可能会对特定细胞类型或条件下的ZNF703表达产生间接影响。 | ||||||
Temozolomide | 85622-93-1 | sc-203292 sc-203292A | 25 mg 100 mg | $89.00 $250.00 | 32 | |
作为烷化剂,替莫唑胺可能会影响DNA损伤反应,并间接调节ZNF703的表达。 | ||||||
5-Aza-2′-Deoxycytidine | 2353-33-5 | sc-202424 sc-202424A sc-202424B | 25 mg 100 mg 250 mg | $214.00 $316.00 $418.00 | 7 | |
DNA甲基转移酶抑制剂可以影响基因的甲基化状态,如果它在甲基化依赖机制中起作用,则可以间接影响ZNF175。 | ||||||
Nutlin-3 | 548472-68-0 | sc-45061 sc-45061A sc-45061B | 1 mg 5 mg 25 mg | $56.00 $212.00 $764.00 | 24 | |
MDM2抑制剂可激活p53,从而影响ZNF175可能参与的转录网络。 |