Fig. 1.
Fig. 1. Morphologic characterization of adherent cells. / (A) CD133+ cells mobilized from peripheral blood were enriched by MACS. Flow cytometry showed that the purity of the positively selected CD133+ cells was generally greater than 99.5%. (B) Inverse microscopic image of typical 6-week-old adherent cells (original magnification, × 200). B indicates bud; M, magnupodium; T, tenupodium. (C) Raster electron micrograph of a 6-week-old adherent cell (original magnification, × 2000). B indicates a bud on the cell surface; L, a spoonlike lobopodium at the terminus of the cell (upper left corner of the micrograph). (D) A 6-week-old adherent cell that emerged from a population of EGFP-expressing CD133+ cells is counterstained with PE-conjugated mouse antihuman CD133 antibody. Yellow fluorescence caused by the overlay of green (EGFP) and red (CD133) fluorescence indicates double staining of the buds (indicated by B).

Morphologic characterization of adherent cells.

(A) CD133+ cells mobilized from peripheral blood were enriched by MACS. Flow cytometry showed that the purity of the positively selected CD133+ cells was generally greater than 99.5%. (B) Inverse microscopic image of typical 6-week-old adherent cells (original magnification, × 200). B indicates bud; M, magnupodium; T, tenupodium. (C) Raster electron micrograph of a 6-week-old adherent cell (original magnification, × 2000). B indicates a bud on the cell surface; L, a spoonlike lobopodium at the terminus of the cell (upper left corner of the micrograph). (D) A 6-week-old adherent cell that emerged from a population of EGFP-expressing CD133+ cells is counterstained with PE-conjugated mouse antihuman CD133 antibody. Yellow fluorescence caused by the overlay of green (EGFP) and red (CD133) fluorescence indicates double staining of the buds (indicated by B).

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