We describe a plate-based cloning and expression strategy for efficient high-throughput generation of validated expression clones in Escherichia coli. The process incorporates 48- or 96-well plates at all stages including the cloning and colony selection phases which are often performed manually. A 48-grid agar growth plate has been integrated into the colony selection component to improve throughput at the cloning stage. The combinations of 48- and 96-well plate formats are compatible with automated liquid handlers and multichannel pipettes. This revised cloning and expression pipeline increases throughput significantly, and also results in a reduction in both time and material requirements. The system has been validated by the production and screening of several thousand clones at the Midwest Center for Structural Genomics.
"System 48" high-throughput cloning and protein expression analysis.
“System 48”高通量克隆和蛋白质表达分析
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作者:Abdullah James M, Joachimiak Andrzej, Collart Frank R
| 期刊: | Methods in Molecular Biology | 影响因子: | 0.000 |
| 时间: | 2009 | 起止号: | 2009;498:117-27 |
| doi: | 10.1007/978-1-59745-196-3_8 | 研究方向: | 免疫/内分泌 |
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