| 生物活性 | |||
|---|---|---|---|
| 描述 | Bractoppin is a potent and selective inhibitor of phosphopeptide recognition by the human BRCA1 tandem BRCT domain (IC50: 74 nM). It reduces BRCA1 recruitment to DNA breaks, thereby suppressing damage-induced G2 arrest and assembly of the recombinase, RAD51. Bractoppin predominantly inhibits BRCA1 tBRCT-dependent processes in the DNA damage response[1]. | ||
| 实验方案 | |||
|---|---|---|---|
| 1mg | 5mg | 10mg | |
|
1 mM 5 mM 10 mM |
2.41mL 0.48mL 0.24mL |
12.06mL 2.41mL 1.21mL |
24.13mL 4.83mL 2.41mL |
| 参考文献 |
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