Automated 96-well format high throughput colony formation assay for siRNA library screen

被引:0
|
作者
Hatch, Stephanie B. [1 ]
Prevo, Remko [2 ]
Chan, Tiffany [2 ]
Millar, Val [1 ]
Cornelissen, Bart [2 ]
Higgins, Geoff [2 ]
Ebner, Daniel [1 ]
机构
[1] Univ Oxford, Target Discovery Inst, Nuffield Dept Med, Oxford, England
[2] Univ Oxford, Dept Biol, Oxford, England
来源
STAR PROTOCOLS | 2022年 / 3卷 / 02期
基金
英国医学研究理事会;
关键词
Cancer; Cell Biology; Cell culture; Cell-based Assays; High Throughput Screening; Molecular Biology; Single Cell;
D O I
10.1016/j.xpro.2022.101355
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The colony formation assay is the gold-standard technique to assess cell viability after treatment with cytotoxic reagents, ionizing radiation, and cytotoxic combinatorial treatments. This protocol describes a high-throughput automated and high-content imaging approach to screen siRNA molecular libraries in HeLa cervical cancer cells in 96-well format. We detail reverse transfection of cells with siRNAs, followed by ionizing radiation, fixing, and staining of the plates for automated colony counting. This protocol can be used across a broad range of cell types. For complete details on the use and execution of this protocol, please refer to Tiwana et al. (2015).
引用
收藏
页数:16
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