Figure 2.
Surface α1-3 fucosylation of CB CD34+ cells with exogenous FTVI and GDP fucose increases sLex epitopes. CB CD34+ cells were incubated in the presence or absence of FTVI and GDP fucose. The cells were then incubated with PE-conjugated anti-CD34 mAb and with anti-sLex mAb HECA-452 identified with a FITC-conjugated second antibody. Binding was measured by flow cytometry. Cells incubated with isotype-matched control antibodies were used to determine fluorescence thresholds for specific binding. The results are representative of 5 independent experiments. The percentage of cells in each quadrant is indicated.

Surface α1-3 fucosylation of CB CD34+ cells with exogenous FTVI and GDP fucose increases sLex epitopes. CB CD34+ cells were incubated in the presence or absence of FTVI and GDP fucose. The cells were then incubated with PE-conjugated anti-CD34 mAb and with anti-sLex mAb HECA-452 identified with a FITC-conjugated second antibody. Binding was measured by flow cytometry. Cells incubated with isotype-matched control antibodies were used to determine fluorescence thresholds for specific binding. The results are representative of 5 independent experiments. The percentage of cells in each quadrant is indicated.

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