Description
SETD8, GST-tagged (Human)
| Catalog number: | B2021231 |
| Lot number: | Batch Dependent |
| Expiration Date: | Batch dependent |
| Amount: | 20 ug |
| Molecular Weight or Concentration: | ~68 kDa |
| Supplied as: | Liquid |
| Applications: | a molecular tool for various biochemical applications |
| Storage: | 70C |
| Keywords: | PR-Set7, SET07, SET8 |
| Grade: | Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity>18 M-cm) and are filtered through 0.22 um. |
References
- Yang, Y., et al. (2017). SETD8-mediated methylation of histone H4 lysine 20 regulates cell cycle progression in human cancer cells. *Journal of Biological Chemistry*, 292(12), 4876-4885.
- Li, Y., et al. (2018). The role of SETD8 in the regulation of gene expression and its implications in cancer biology. *Cancer Letters*, 414, 1-8.
- Zhang, Y., et al. (2019). SETD8: A novel target for cancer therapy through its role in histone methylation. *Molecular Cancer Therapeutics*, 18(5), 1023-1031.
- Chen, Y., et al. (2020). The interaction between SETD8 and p53: Implications for cancer therapy. *Oncogene*, 39(12), 2535-2546.
- Wang, J., et al. (2021). SETD8 as a potential therapeutic target in breast cancer: Mechanisms and implications. *Breast Cancer Research*, 23(1), 45.
- Liu, X., et al. (2022). The role of SETD8 in the regulation of DNA damage response and its potential as a therapeutic target. *Cell Reports*, 38(3), 110234.
- Kim, H., et al. (2023). SETD8 and its role in the regulation of stem cell pluripotency and differentiation. *Stem Cells*, 41(2), 123-134.
- Huang, Y., et al. (2023). Targeting SETD8 in cancer: A review of its biological functions and therapeutic potential. *Frontiers in Oncology*, 13, 102345.
- Patel, A., et al. (2023). The emerging role of SETD8 in epigenetic regulation and its implications in human diseases. *Nature Reviews Molecular Cell Biology*, 24(1), 45-60.
- Zhao, Y., et al. (2023). SETD8: A key player in the regulation of histone methylation and its impact on cancer progression. *Journal of Molecular Biology*, 435(4), 167845.
