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Updated: Dec 29, 2025

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Published on: August 26, 2021
DWH24: a new antibody for fluorescence-based cell death analysis
Anna Ryschich1, Yan Dong1, Michael Schäfer1
1Section of Surgical Research, Clinic of General, Visceral and Transplantation Surgery, University of Heidelberg, Heidelberg, Germany.
Insights
A new antibody, DWH24, effectively visualizes and quantifies dead cells using fluorescence imaging and flow cytometry. This tool offers a cost-effective and universal method for analyzing cell death progression in various conditions.
Area of Science:
- Immunology
- Cell Biology
Background:
- Antibodies are crucial in diagnostics and therapeutics.
- Current cell death markers have limitations.
Purpose of the Study:
- To develop and characterize a novel antibody clone, DWH24.
- To evaluate DWH24's utility in visualizing and quantifying cell death.
Main Methods:
- Targeted and cell immunization approaches for antibody development.
- Immunofluorescence, fluorescence microscopy, and flow cytometry for characterization.
- Time-lapse microscopy for live imaging of cell death.
- Human proteome microarray for specificity analysis.
Main Results:
- DWH24 is an IgM kappa (IgMκ) antibody.
- It enables excellent visualization and quantification of dead cells.
- Binding is Ca2+- and protein-independent, allowing live imaging.
- Specificity analysis revealed binding to tropomyosin variants and FAM131C.
Conclusions:
- DWH24 is a valuable tool for cell death analysis.
- It offers a cost-effective and universal approach using fluorescence imaging and flow cytometry.
- The antibody facilitates live imaging of cell death dynamics.
Abstract:
Antibodies have gained considerable importance in laboratory and clinical settings. Currently, antibodies are extensively employed for the diagnosis and treatment of several human diseases. Herein, using targeted and cell immunisation approaches, we developed and characterised an antibody clone, DWH24. We found that DWH24 is an IgMκtype antibody that enables excellent visualisation and quantification of dead cells using immunofluorescence, fluorescence microscopy, and flow cytometry. This property was proved by the spontaneous cell death of several tumour cell lines and stimulated T cells, as well as after chemo- and photodynamic therapy. Unlike conventional apoptosis and cell death markers, DWH24 binding occurred in a Ca2+- and protein-independent manner and enabled live imaging of cell death progress, as shown using time-lapse microscopy. The binding specificity of DWH24 was analysed using a human proteome microarray, which revealed a complex response profile with very high spot intensities against various proteins, such as tropomyosin variants and FAM131C. Accordingly, DWH24 can be employed as a suitable tool for the cost-effective and universal analysis of cell death using fluorescence imaging and flow cytometry.
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