Table 1.

Relative expression of CD164 epitopes on CD34 and AC133 subsets of human fetal liver cells

Cell Subset % CD34 Cells Expressing CD164 and AC133 Epitopes (mean ± SD; n = 3)Median Fluorescence Intensity of CD164 Labeling for Each Specified CD34+AC133 Subset (mean ± SD; n = 3)
Class I 105A5 Class II 103B2/9E10 Class III N6B6 Class I 105A5 Class II 103B2/9E10Class III N6B6
CD34+AC133+CD164+ 58 ± 14  79 ± 4  79 ± 5  40 ± 12 259 ± 128  205 ± 104 
CD34+AC133loCD164+ 12 ± 8  15 ± 7  17 ± 7  36 ± 9 133 ± 11  99 ± 31 
CD34+AC133+CD164lo 21 ± 12  2 ± 0  1 ± 0  11 ± 1 11 ± 0  12 ± 1 
CD34+AC133loCD164lo 9 ± 2  5 ± 3  3 ± 2  7 ± 1  6 ± 0 10 ± 1 
Cell Subset % CD34 Cells Expressing CD164 and AC133 Epitopes (mean ± SD; n = 3)Median Fluorescence Intensity of CD164 Labeling for Each Specified CD34+AC133 Subset (mean ± SD; n = 3)
Class I 105A5 Class II 103B2/9E10 Class III N6B6 Class I 105A5 Class II 103B2/9E10Class III N6B6
CD34+AC133+CD164+ 58 ± 14  79 ± 4  79 ± 5  40 ± 12 259 ± 128  205 ± 104 
CD34+AC133loCD164+ 12 ± 8  15 ± 7  17 ± 7  36 ± 9 133 ± 11  99 ± 31 
CD34+AC133+CD164lo 21 ± 12  2 ± 0  1 ± 0  11 ± 1 11 ± 0  12 ± 1 
CD34+AC133loCD164lo 9 ± 2  5 ± 3  3 ± 2  7 ± 1  6 ± 0 10 ± 1 

Purified CD34+ cells from fetal liver cells were labeled with CD34-PerCP, AC133-PE, and the different CD164 MAbs plus FITC-conjugated anti-isotype secondary antibodies as described in “Materials and methods.” The percentages of cells falling within each quadrant were determined by comparison with the negative isotype-matched control MAbs. Values represent means ± SD of 3 independent experiments.

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