表达重组靶点（如单克隆抗体、孔通道和 GPCRs）的稳定和瞬转细胞系常用于药物筛选、基因功能研究、细胞系筛选和安全评估研究。细胞系的开发过程从将感兴趣的质粒载体转染选定的宿主细胞（通常是 CHO 或 HEK 293 细胞）开始，然后根据细胞功能、产量和/或稳定性进行筛选和压力选择。选择后，根据它们的应用，细胞系和/或细胞产生的蛋白质被验证有效。由于手动筛选方法耗时、耗力且容易出错，因此对高通量、自动化筛选解决方案的需求很大。
贝克曼库尔特的 Biomek 工作站提供一套全方位的高通量自动化平台，可轻松整合，以满足细胞系开发工作流的每个关键步骤。
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PRODUCT AVAILABILITY AND REGULATORY STATUS DEPENDS ON COUNTRY REGISTRATION PER APPLICABLE REGULATIONS
The listed regulatory status for products correspond to one of the below:
IVD: In Vitro Diagnostic Products. These products are labeled "For In Vitro Diagnostic Use."
ASR: Analyte Specific Reagents. These reagents are labeled "Analyte Specific Reagents. Analytical and performance characteristics are not established."
CE: Products intended for in vitro diagnostic use and conforming to European Directive (98/79/EC). (Note: Devices may be CE marked to other directives than (98/79/EC)
RUO: Research Use Only. These products are labeled "For Research Use Only. Not for use in diagnostic procedures."
LUO: Laboratory Use Only. These products are labeled "For Laboratory Use Only."
No Regulatory Status: Non-Medical Device or non-regulated articles. Not for use in diagnostic or therapeutic procedures.
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