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Automated antibody dispensing to improve high‐parameter flow cytometry throughput and analysis

Over the past decade, the flow cytometry field has witnessed significant advancements in the number of fluorochromes that can be detected. This enables researchers to analyze more than 40 markers simultaneously on thousands of cells per second. However, with this increased complexity and multiplicit...

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Published in:Cytometry. Part A 2024-06, Vol.105 (6), p.464-473
Main Authors: Bosteels, Victor, Van Duyse, Julie, Ruyssinck, Elien, Van der Borght, Katrien, Nguyen, Long, Gavel, Jannes, Janssens, Sophie, Van Isterdael, Gert
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container_end_page 473
container_issue 6
container_start_page 464
container_title Cytometry. Part A
container_volume 105
creator Bosteels, Victor
Van Duyse, Julie
Ruyssinck, Elien
Van der Borght, Katrien
Nguyen, Long
Gavel, Jannes
Janssens, Sophie
Van Isterdael, Gert
description Over the past decade, the flow cytometry field has witnessed significant advancements in the number of fluorochromes that can be detected. This enables researchers to analyze more than 40 markers simultaneously on thousands of cells per second. However, with this increased complexity and multiplicity of markers, the manual dispensing of antibodies for flow cytometry experiments has become laborious, time‐consuming, and prone to errors. An automated antibody dispensing system could provide a potential solution by enhancing the efficiency, and by improving data quality by faithfully dispensing the fluorochrome‐conjugated antibodies and by enabling the easy addition of extra controls. In this study, a comprehensive comparison of different liquid handlers for dispensing fluorochrome‐labeled antibodies was conducted for the preparation of flow cytometry stainings. The evaluation focused on key criteria including dispensing time, dead volume, and reliability of dispensing. After benchmarking, the I.DOT, a non‐contact liquid handler, was selected and optimized in more detail. In the end, the I.DOT was able to prepare a 25‐marker panel in 20 min, including the full stain, all FMOs and all single stain controls for cells and beads. Having all these controls improved the validation of the panel, visualization, and analysis of the data. Thus, automated antibody dispensing by dispensers such as the I.DOT reduces time and errors, enhances data quality, and can be easily integrated in an automated workflow to prepare samples for flow cytometry.
doi_str_mv 10.1002/cyto.a.24835
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subjects Antibodies
Antibodies - immunology
antibody pipetting
Automation
Dispensing
Error reduction
Flow cytometry
Flow Cytometry - methods
Fluorescent Dyes - chemistry
Fluorophores
Handlers
High-Throughput Screening Assays - methods
high‐parameter flow cytometry
Humans
I.DOT
Medical research
Reproducibility of Results
Staining and Labeling - methods
Workflow
title Automated antibody dispensing to improve high‐parameter flow cytometry throughput and analysis
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