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A Semi-automated Approach to Preparing Antibody Cocktails for Immunophenotypic Analysis of Human Peripheral Blood
Published on: February 8, 2016
Quality Control of Immunophenotyping
1Department of Pathology, Microbiology, and Immunology, Hematopathology/Flow Cytometry, Vanderbilt University Medical Center, Vanderbilt Medical Laboratories, Nashville, TN, 37228, USA. greigbw@gmail.com.
Abstract:
Applications of flow cytometry and immunophenotyping offer precise and accurate means for providing information used to both diagnose and monitor disease; they serve as a standard platform for many research endeavors that study discrete populations of biological entities. The proper use of this highly sophisticated technology requires daily and ongoing monitoring of both the instrument and the methodology. Best practices for this begin with quality control (QC) procedures designed to set up and monitor the reagents used, the instrument performance, and the results to ensure that they are working properly both on the day of use and over time. If the results of those QC procedures are outside of acceptable, then recording the corrective action taken must also be included in the quality control records. Quality assurance (QA) is a way to know that the three phases of testing, namely, pre-analytic, analytic, and post-analytic procedures, are being followed. This chapter describes the procedures used to assess quality control as it pertains to flow cytometry and immunophenotyping in all three phases of testing.

