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. Author manuscript; available in PMC: 2026 Mar 12.
Published in final edited form as: Clin Cancer Res. 2021 Jan 6;27(7):1932–1940. doi: 10.1158/1078-0432.CCR-20-2725

Figure 2.

Figure 2.

Flow cytometry of the mTIGIT receptor. A, HeLa cells transfected with a plasmid expressing the mTIGIT receptor were stained with PE-TIGIT (light blue) or PE-IgG (red). B, Quantitative flow on transfected TIGIT-expressing cells shows an average of 9.5 × 104 receptors per cell. C, Live cell binding assay for the determination of binding specificity of TIGITmAb and DFO-TIGITmAb on activated mouse splenocytes. Splenocytes were activated with PMA and calcium ionomycin (50:500 ng/mL for 4 hours). Cells (1 × 106) were stained with isotype control mouse IgG, TIGIT-mAb or DFO-TIGITmAb, followed by anti-mouse-IgG APC staining. Histogram traces correspond to induced splenocytes stained with the following mAbs (1 μg/0.1 mL): mouse IgG isotype control (open histogram), DFO-TIGITmAb (dotted histogram), and unmodified TIGITmAb (filled histogram) for TIGIT expression.