Figure 1.
Figure 1. ALDHbr CD34+, ALDHneg CD34+, and ALDHbr CD34neg cells derived from UCB. UCB cells were labeled with BAAA, as described in “Materials and methods.” (A) Background fluorescence was established in the presence of DEAB. (B,E) SSClo ALDHneg and SSClo ALDHbr cell fractions were defined. (C-D) Both cell fractions contained CD34+ cells, although the SSClo ALDHbr fraction was highly enriched for CD34+ cells, to include CD34+ CD38neg cells (n = 8) (D). In most developmental studies, cells expressing lineage-specific antigens were excluded (n = 25). (F) CD34+ linneg cells were isolated from the SSClo ALDHneg. (G) CD34+ linneg and CD34neg linneg cells were isolated from SSClo ALDHbr UCB (H-M). To ensure purity, each cell fraction was sorted twice. Representative reanalyses depict twice-purified linneg SSClo ALDHneg CD34+ cells (H,K), linneg SSClo ALDHbr CD34neg cells (I,L), and linneg SSClo ALDHbr CD34+ cells (J,M).

ALDHbr CD34+, ALDHneg CD34+, and ALDHbr CD34neg cells derived from UCB. UCB cells were labeled with BAAA, as described in “Materials and methods.” (A) Background fluorescence was established in the presence of DEAB. (B,E) SSClo ALDHneg and SSClo ALDHbr cell fractions were defined. (C-D) Both cell fractions contained CD34+ cells, although the SSClo ALDHbr fraction was highly enriched for CD34+ cells, to include CD34+ CD38neg cells (n = 8) (D). In most developmental studies, cells expressing lineage-specific antigens were excluded (n = 25). (F) CD34+ linneg cells were isolated from the SSClo ALDHneg. (G) CD34+ linneg and CD34neg linneg cells were isolated from SSClo ALDHbr UCB (H-M). To ensure purity, each cell fraction was sorted twice. Representative reanalyses depict twice-purified linneg SSClo ALDHneg CD34+ cells (H,K), linneg SSClo ALDHbr CD34neg cells (I,L), and linneg SSClo ALDHbr CD34+ cells (J,M).

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