Chromatin/Epigenetics
Chromatin/Epigenetics(染色质/表观遗传学)
Epigenetics
Epigenetics means above genetics. It determines how much and whether a gene is expressed without changing DNA sequences. Epigenetic regulations include, 1. DNA methylation: the addition of methyl group to DNA, converting cytosine to 5-methylcytosine, mostly at CpG sites; 2. Histone modifications: posttranslational modificationEpigeneticss of histone proteins including acetylation, methylation, ubiquitylation, phosphorylation and sumoylation; 3. miRNAs: non-coding microRNA downregulating gene expression; 4. Prions: infectious proteins viewed as epigenetic agents capable of inducing a phenotype without changing the genome.
- Bromodomain(50)
- Aurora Kinase(63)
- DNA Methyltransferase(35)
- HDAC(210)
- Histone Acetyltransferases(78)
- Histone Demethylases(110)
- Histone Methyltransferase(240)
- HIF(102)
- JAK(173)
- MBT Domains(1)
- PARP(122)
- Pim(32)
- Protein Ser/Thr Phosphatases(34)
- RNA Polymerase(7)
- Sirtuin(77)
- Sphingosine Kinase-2(1)
- Polycomb repressive complex(2)
- SUMOylation(3)
- PAD(21)
- Epigenetic Reader Domain(246)
- MicroRNA(24)
- Protein Arginine Deiminase(7)
- Chromodomain(1)
- Citrullination(20)
- DNA/RNA Demethylation(2)
- DNA/RNA Methylation(8)
- Histone Deacetylation(44)
- Histones/Histone Peptides(62)
- PHD Domains(1)
- Tandem Tudor & Tudor-like Domains(1)
- PRMT(2)
- Readers(1)
- Small Interfering RNA (siRNA)(1)
- METTL3(2)
- WDR5(1)
- TET Protein(2)
- HuR(1)
- SF3B1(1)
Chromatin/Epigenetics 相关产品(1617)
- GC13926BMS-345541(free base)CAS: 445430-58-0纯度: >99.50%
BMS-345541(free base) 是 IKK 催化亚基的选择性抑制剂 (IKK-2 IC50=0.3 μM, IKK-1 IC50=4 μM)。 BMS-345541(游离碱)结合在 IKK 的变构位点。
| 货号 | 产品名称 | CAS号 | 纯度 | 结构 |
|---|---|---|---|---|
| GC11095 | Pyroxamide | 382180-17-8 | >99.50% | |
A HDAC inhibitor | ||||
| GC13591 | TC-H 106 | 937039-45-7 | >98.00% | |
A tight-binding inhibitor of class I HDACs | ||||
| GC10676 | AK-7 | 420831-40-9 | >99.50% | |
An inhibitor of SIRT2 | ||||
| GC11375 | UNC1999 | 1431612-23-5 | >99.50% | |
UNC1999是一种口服活性的EZH2(IC 50 =2nM)和EZH1(IC 50 =45nM)抑制剂。 | ||||
| GC11424 | Valproic acid | 99-66-1 | >98.00% | |
A class I HDAC inhibitor | ||||
| GC12667 | 4SC-202 | 1186222-89-8 | >99.50% | |
An HDAC1-3 and KDM1A inhibitor | ||||
| GC13764 | Nexturastat A | 1403783-31-2 | >98.00% | |
A potent, cell-permeable HDAC6 inhibitor | ||||
| GC13926 | BMS-345541(free base) | 445430-58-0 | >99.50% | |
BMS-345541(free base) 是 IKK 催化亚基的选择性抑制剂 (IKK-2 IC50=0.3 μM, IKK-1 IC50=4 μM)。 BMS-345541(游离碱)结合在 IKK 的变构位点。 | ||||
| GC14652 | MM-102 | 1417329-24-8 | >98.00% | |
MM-102是一种高亲和性、细胞通透性的肽模拟物,作为MLL1-WDR5蛋白相互作用的有效抑制剂,IC₅₀为2.4nM,K i <1nM。 | ||||
