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Resolution: standard / high Figure 3.
PEs surface recognition. a. Anti-var2CSA DBL mouse sera were tested for surface recognition of erythrocytes
infected with parasites of the FCR3, 7G8 and HB3 strains with CSA- and CD36 binding
phenotypes, respectively. Analysis was performed using flow cytometry and fluorescence
microscopy. A representative example of a specific surface immunolabeling using the
DBL6-1 antisera and the corresponding differential interferential contrast microscopy
field are shown. Flow cytometry data shown are the normalized geometric mean fluorescence
index (MFI) (± SD) obtained by subtracting the preimmune MFI value from the immune
MFI value. b. Alignment of the DBL6-ε var2CSA sequences from the 3 parasite lines
used to assess the antisera cross-reactivity by FACS. Conserved residues between FCR3
sequence and the other sequences are boxed with a yellow background.
Fernandez et al. Malaria Journal 2008 7:170 doi:10.1186/1475-2875-7-170 |