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As shown in Figure 5A, the fluorescence signal of the tumor region gradually increased with time and reached a plateau at 6 h post-injection, which provided a basis for us to select the optimal illumination time
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CyTOF Metal-isotope conjugated monoclonal antibodies (Supplementary Data 2) targeting T cell phenotypic, activation, and metabolic proteins were used to evaluate the metabolic and activation properties of patient-derived CAR T cells in vitro and ex vivo
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