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. Author manuscript; available in PMC: 2020 Feb 4.
Published in final edited form as: Angew Chem Int Ed Engl. 2019 Jan 14;58(6):1621–1625. doi: 10.1002/anie.201809010

Figure 2.

Figure 2.

Analysis and verification of ZAP-1-targeted protein. (a) Flow cytometry of FAM-labelled initial library (red) and ZAP-1 (blue) with MDA-MB-231 cells treated with proteinase K (orange) and trypsin (green). (b) SDS-PAGE was used to identify ZAP-1-specific band T1, marked as asterisk. 1, marker; 2, cell lysate; 3, beads only; 4, proteins captured by initial library; 5, proteins captured by ZAP-1. (c) Fluorescence confocal images of MDA-MB-231 cells incubated with ZAP-1 and anti-ITGA3. (Scale bar, 50 μm.)