Trichostatin A | HDAC inhibitor
NMR (Conforms)
Available Options
| Size : | Price | Quantity | |
|---|---|---|---|
| 1 mg | $78.00 | ||
| 5 mg | $220.00 |
Trichostatin A (58880-19-6) is a potent and selective histone deacetylase (HDAC) inhibitor (Ki = 3.4 nM). Induces reversion of ras transformed cells to normal morphology. Trichostatin A induces dedifferentiation of primordial germ cells into embryonic germ cells. Cell permeable and active in vivo. Decreased global chromatin condensation increasing gene-editing efficiency 2-4X.4 Part of the CRISPY mix for increasing precise gene editing.5
References/Citations:
1) Yoshida et al. (1990), Potent and specific inhibition of mammalian histone deacetylase both in vivo and in vitro by trichostatin A ; J. Biol. Chem., 265 17174
2) Futamura et al. (1995), Trichostatin A inhibits both ras-induced neurite outgrowth of PC12 cells and morphological transformation of NIH3T3 cells; Oncogene, 10 1119
3) Durcova-Hills et al. (2008), Reprogramming Primordial Germ Cells into Pluripotent Stem Cells; PLoS-One, 3 e3531
4) Molugu et al. (2023), Trichostatin A for Efficient CRISPR-Cas9 Gene Editing of Human Pluripotent Stem Cells; CRISPR J., 6 473
5) Riesenberg and Maricic (2018), Targeting repair pathways with small molecules increases precise genome editing in pluripotent stem cells; Nat. Commun., 9 2165
NMR (Conforms)
Safety Data Sheet:
Product Data Sheet:
Materials provided by Focus Biomolecules are for laboratory research use only and are not intended for human or veterinary applications. Please note that we do not sell to individuals and that all orders placed by non-research organizations will incur a $20 restocking/refund fee
Trichostatin A (58880-19-6) is a potent and selective histone deacetylase (HDAC) inhibitor (Ki = 3.4 nM). Induces reversion of ras transformed cells to normal morphology. Trichostatin A induces dedifferentiation of primordial germ cells into embryonic germ cells. Cell permeable and active in vivo. Decreased global chromatin condensation increasing gene-editing efficiency 2-4X.4 Part of the CRISPY mix for increasing precise gene editing.5
References/Citations:
1) Yoshida et al. (1990), Potent and specific inhibition of mammalian histone deacetylase both in vivo and in vitro by trichostatin A ; J. Biol. Chem., 265 17174
2) Futamura et al. (1995), Trichostatin A inhibits both ras-induced neurite outgrowth of PC12 cells and morphological transformation of NIH3T3 cells; Oncogene, 10 1119
3) Durcova-Hills et al. (2008), Reprogramming Primordial Germ Cells into Pluripotent Stem Cells; PLoS-One, 3 e3531
4) Molugu et al. (2023), Trichostatin A for Efficient CRISPR-Cas9 Gene Editing of Human Pluripotent Stem Cells; CRISPR J., 6 473
5) Riesenberg and Maricic (2018), Targeting repair pathways with small molecules increases precise genome editing in pluripotent stem cells; Nat. Commun., 9 2165
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