CDK9 is an attractive target for cancer therapeutics due to its crucial role in transcription regulation, particularly of short-lived anti-apoptotic proteins such as MCL-1 and XIAP which are critical to the survival of cancer cells. One approach for specifically degrading CDK9 is using a proteolysis targeting chimera (PROTAC).
In this application note, you will discover:
For research use only. Not for use in diagnostic procedures.
CDK signaling in oncology: assess the effectiveness of a CDK9-targeting PROTAC molecule