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Protocol for assessing anti-Siglec-9 antibody-mediated tumor phagocytosis by macrophages using pH-sensitive dyes and flow cytometry

The protocol standardises monocyte isolation, macrophage differentiation, K562 preparation and pH-sensitive flow cytometry to distinguish binding from internalisation. It improves mechanistic reproducibility but does not demonstrate patient efficacy or safety.

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Key findings

  • The protocol standardises monocyte isolation, macrophage differentiation, K562 preparation and pH-sensitive flow cytometry to distinguish binding from internalisation. It improves mechanistic reproducibility but does not demonstrate patient efficacy or safety.
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Why this matters globally

This work adds internationally comparable evidence in Health sciences and defines questions for replication in other populations or systems. Its global value lies in the evidence and transferable reasoning, not in a single impact score.

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Thai researcher contribution

Thailand-linked authors and Siriraj Hospital, Mahidol University contribute to the research network behind this work. Thai participation is identified from bibliographic affiliations and should be checked against the author list and source article.

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Limitations to consider

Method readiness is not intervention efficacy; inter-laboratory reproducibility and downstream outcome studies are still required.

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Verify the original sources

STAR ProtocolsRead the original article

DOI: 10.1016/j.xpro.2026.104590

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