Flow Cytometry Core Facility, Vaccine Research Center, National Institute of Allergy and Infectious Diseases (NIAID), National Institutes of Health (NIH), Bethesda, MD, USA.
Nat Protoc. 2012 Dec;7(12):2067-79. doi: 10.1038/nprot.2012.126. Epub 2012 Nov 8.
The quality assurance program presented here provides a means to maximize and maintain the performance of individual flow cytometers in a facility. To optimize performance, we recommend performing all three steps (optimization, calibration and standardization) in this program when a new flow cytometer is installed or whenever the flow cytometer's optical path is altered (e.g., lasers, filters or detectors are replaced). The complete process requires 3-4 h. On a more frequent basis, only a subset of these procedures need to be performed as a part of daily maintenance routines. The data generated can be tracked to monitor the instrument and determine whether service is needed. In addition, the data can provide a metric for whether repairs and upgrades have improved or harmed performance, and for future instrument-to-instrument comparisons. In sum, the procedures presented here represent an updated framework for optimizing, calibrating and standardizing a flow cytometer for daily use.
这里介绍的质量保证程序提供了一种在设施中最大限度地提高和维持各个流式细胞仪性能的方法。为了优化性能,我们建议在安装新的流式细胞仪或流式细胞仪的光路发生变化(例如,更换激光器、滤光片或检测器)时,执行该程序中的所有三个步骤(优化、校准和标准化)。整个过程需要 3-4 小时。在更频繁的基础上,作为日常维护程序的一部分,只需要执行这些步骤的一部分。生成的数据可以进行跟踪,以监测仪器并确定是否需要进行维护。此外,该数据可以提供一个衡量标准,用于确定维修和升级是否提高或损害了性能,并用于未来的仪器间比较。总之,这里介绍的程序代表了一个用于优化、校准和标准化流式细胞仪以进行日常使用的更新框架。