抗体工程-融合流程通过数据驱动和控制流程管理，实现自动化骨髓瘤细胞培养，自动化加入需要大量人力且时间敏感的培养基添加步骤。
该系统采用 SAMI EX 时序优化软件对工作流步骤进行优化。此外，该系统还包括用于更大容量的实验室耗材堆栈、两个孵育模块（用于在两个不同的温度），以及一个整合的 Vi-Cell XR 细胞活力分析仪和一个用于换培养基的微孔板离心机。
下面展示的系统是一个整合的 Biomek i7 液体处理工作站的示例，该工作站专门为有效的管理杂交瘤筛选过程中细胞融合步骤所设计。该系统配置可以根据您的特定工作流的要求进行修改，以适应其他分析方法或实验应用。
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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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