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. Author manuscript; available in PMC: 2013 Oct 31.
Published in final edited form as: J Immunol Methods. 2012 Jul 20;384(1-2):43–50. doi: 10.1016/j.jim.2012.07.003

Figure 1.

Figure 1

Analysis of sLex microspheres by flow cytometry. The sLex microspheres were first treated with HECA-452 and then a FITC labeled goat anti-rat IgM antibody. The histograms represent the fluorescence distribution of the population of microspheres analyzed. The log fluorescence correlates with the levels of HECA-452 epitopes bound to the sLex microspheres. The coating concentrations used to prepare the sLex microspheres are shown on the right side. The data presented represent n≥3 experiments.