摘要
A microfluidic chip based method utilized for effective screening of high-throughput peptide libraries was achieved. Continuous flow bead trapping, sorting, arraying and in situ sequencing was integrated. Peptide library screening with 105 beads was processed within 4 hours and peptide ligands toward the target protein AHA and APN were successfully discovered.
| 源语言 | 英语 |
|---|---|
| 页(从-至) | 61767-61770 |
| 页数 | 4 |
| 期刊 | RSC Advances |
| 卷 | 4 |
| 期 | 106 |
| DOI | |
| 出版状态 | 已出版 - 2014 |
| 已对外发布 | 是 |
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