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. Author manuscript; available in PMC: 2017 Jul 5.
Published in final edited form as: Bio Protoc. 2016 Sep 20;6(18):e1927. doi: 10.21769/BioProtoc.1927

Figure 1. Labeling efficiency of FLARE conidia.

Figure 1

Flow plots depict fluorescence intensity of (A) unlabeled, (B) AF633-labeled, (C) DsRed-labeled, and (D) FLARE conidia in AF633 (X-axis) and DsRed (Y-axis) channels using a BD LSR II flow cytometer equipped with 532 nm and 633 nm lasers.