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Flow cytometry data was analyzed utilizing the Gore lab's flow cytometry tool kit, which can be accessed at http://gorelab.bitbucket.org/flowcytometrytools/.
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This present study showed clearly that online flow cytometry is an advantageous tool for the real-time monitoring of microbial culture at a single-cell level.
Flow cytometry is a powerful tool for quantitative biology because it can perform single-cell analysis of large cell populations using multiple parameters.
This assay, with a user-friendly protocol that has many similarities to standard antibody-staining procedures and data acquisition of flow cytometry, is an invaluable tool for any immunology lab performing translational research.
We sought to establish flow cytometry as a novel tool for pancreas research that can complement prevailing advanced microscopic techniques.
In summary, multiparameter intracellular flow cytometry is a valuable tool to assess signaling status quantitatively in a variety of lymphoctye populations.
Flow cytometry is a powerful tool for quantitative, single-cell analysis and can be used for ultra-high-throughput analysis and sorting for multiple markers of interest.
Multi-parameter flow cytometry is a powerful tool for assaying intracellular levels of phosphoproteins and can be used to simultaneously determine immunophenotype and signaling activity in individual cells.
Flow cytometry represents a valuable tool to investigate the influences of cultivation conditions and process variations on virus replication and virus yields.
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