Automated antibody dispensing to improve high-parameter flow cytometry throughput and analysis
- PMID: 38456613
- DOI: 10.1002/cyto.a.24835
Automated antibody dispensing to improve high-parameter flow cytometry throughput and analysis
Abstract
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.
Keywords: I.DOT; antibody pipetting; automation; high‐parameter flow cytometry.
© 2024 The Authors. Cytometry Part A published by Wiley Periodicals LLC on behalf of International Society for Advancement of Cytometry.
References
REFERENCES
-
- Mair F, Prlic M. OMIP‐044: 28‐color immunophenotyping of the human dendritic cell compartment. Cytometry A. 2018;93:402–405.
-
- Nettey L, Giles AJ, Chattopadhyay PK. OMIP‐050: a 28‐color/30‐parameter fluorescence flow cytometry panel to enumerate and characterize cells expressing a wide array of immune checkpoint molecules. Cytometry A. 2018;93:1094–1096.
-
- Park LM, Lannigan J, Jaimes MC. OMIP‐069: forty‐color full spectrum flow cytometry panel for deep immunophenotyping of major cell subsets in human peripheral blood. Cytometry A. 2020;97:1044–1051.
-
- Sahir F, Mateo JM, Steinhoff M, Siveen KS. Development of a 43 color panel for the characterization of conventional and unconventional T‐cell subsets, B cells, NK cells, monocytes, dendritic cells, and innate lymphoid cells using spectral flow cytometry. Cytometry A. 2024;105(5):404–410. https://doi.org/10.1002/cyto.a.24288
-
- Konecny AJ, Mage P, Tyznik AJ, Prlic M, Mair F. 50‐color phenotyping of the human immune system with in‐depth assessment of T cells and dendritic cells. 2023 http://biorxiv.org/lookup/doi/10.1101/2023.12.14.571745
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Miscellaneous