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。
NOT ALL PRODUCTS ARE AVAILABLE IN ALL COUNTRIES.
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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