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Related Experiment Video

Updated: Dec 3, 2025

Mass Cytometry Analysis of Systemic and Local Immune Responses in Hepatocellular Carcinoma
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Mass Cytometry Analysis of Systemic and Local Immune Responses in Hepatocellular Carcinoma

Published on: April 25, 2025

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High-Throughput Mass Cytometry Staining for Immunophenotyping Clinical Samples.

Emily M Thrash1, Katja Kleinsteuber1, Emma S Hathaway1

  • 1Center for Immuno-Oncology, Dana-Farber Cancer Institute, Boston, MA 02215, USA.

STAR Protocols
|October 28, 2020
PubMed
Summary
This summary is machine-generated.

This study introduces a streamlined mass cytometry (MC) workflow using reference sample spike-in and cell barcoding to reduce batch effects. The method ensures reproducible data for up to 80 samples in high-throughput clinical settings.

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Area of Science:

  • Biomedical research
  • Clinical diagnostics
  • Immunology

Background:

  • Implementing mass cytometry (MC) in clinical settings requires robust protocols to minimize batch effects.
  • Reproducibility is crucial for reliable clinical data interpretation.

Purpose of the Study:

  • To present a streamlined, high-throughput mass cytometry workflow.
  • To reduce batch effects and improve data reproducibility in clinical MC applications.

Main Methods:

  • Developed a workflow combining reference sample spike-in and palladium-based mass-tag cell barcoding.
  • Applied the method for high-throughput staining of up to 80 samples per experiment.

Main Results:

  • The workflow generates reproducible data by decreasing experimental variables.
  • Successfully mitigated batch effects in a high-throughput setting.

Conclusions:

  • The presented streamlined MC workflow enhances data reproducibility for clinical implementation.
  • This method is valuable for reducing technical error and batch effects in large-scale sample analysis.