Abstract
Biochemical selectivity profiling is an integral part of early drug development. Typically compounds from optimization phase are regularly tested for off-target activities within or across target families. This article presents workflow and critical aspects of biochemical protein kinase profiling based on microfluidic mobility shift assays.
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Acknowledgment
I would like to thank Shin Numao and Patrik Roethlisberger for their helpful input to the manuscript. I would like to thank Joerg Trappe for suggesting and encouraging the drafting of this manuscript.
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Drueckes, P. (2016). Protein Kinase Selectivity Profiling Using Microfluid Mobility Shift Assays. In: Janzen, W. (eds) High Throughput Screening. Methods in Molecular Biology, vol 1439. Humana Press, New York, NY. https://doi.org/10.1007/978-1-4939-3673-1_9
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DOI: https://doi.org/10.1007/978-1-4939-3673-1_9
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