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Use Case

Plasma from Dog with Bladder Cancer for Cancer Diagnostics & Biomarker Development

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Use Case

Plasma from Dog with Bladder Cancer for Cancer Diagnostics & Biomarker Development

Description

A study evaluated circulating tumor DNA (ctDNA) as a biomarker for monitoring canine urothelial carcinoma, which frequently harbors the BRAF V595E mutation. In 15 dogs with urothelial carcinoma, researchers used real-time PCR to detect and quantify BRAF-mutated ctDNA in plasma. BRAF-mutated ctDNA levels were significantly higher in dogs with the mutation and correlated with disease progression and treatment response. These results suggest that ctDNA analysis could be a useful tool for monitoring urothelial carcinoma in dogs. [Ref: Tagawa, M., Tambo, N., Maezawa, M., Tomihari, M., Watanabe, K., Inokuma, H., & Miyahara, K. (2020). Quantitative analysis of the BRAF V595E mutation in plasma cell-free DNA from dogs with urothelial carcinoma. PLoS ONE, 15(4), e0232365. https://doi.org/10.1371/journal.pone.0232365]

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Cancer Research, Biomarker Development

Related product to Plasma from Dog with Bladder Cancer for Cancer Diagnostics & Biomarker Development

Plasma from Dog with Bladder Cancer for Cancer Diagnostics & Biomarker Development is a Use Case of:

Product: Canine Plasma - Bladder Cancer

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Canine Plasma - Bladder Cancer

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Davide Confalonieri, PhD

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PBMCs are used in antibody discovery due to their role in the immune response. Antibody-secreting cells (ASCs), a type of PBMC, are an excellent source of high-affinity antibodies with therapeutic potential. Millions of PBMCs can be isolated and screened to identify antigen-specific ASCs that secrete antibodies with desirable properties. One method involves microfluidic encapsulation of single ASCs into an antibody capture hydrogel, followed by antigen bait sorting using flow cytometry, enabling the rapid discovery of monoclonal antibodies. These antibodies can then be further characterized for their binding affinity and neutralizing capacity, making PBMCs a valuable resource for developing antibody-based drugs and studying immune responses. [Ref: Fischer, K., Lulla, A., So, T.Y. et al. Rapid discovery of monoclonal antibodies by microfluidics-enabled FACS of single pathogen-specific antibody-secreting cells. Nat Biotechnol (2024). https://doi.org/10.1038/s41587-024-02346-5]

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