Figure 1. Flow cytometric analysis of CD34 and CD38 expression following isolation from human cord blood and long-term coculture with OP9-control cells or OP9-DL1 cells. (A) Human HSCs were isolated into CD34+ and CD34– fractions from human cord blood following a CD34-positive selection protocol on AutoMACS. As a reference for fold enrichment, we show CD34 by CD38 expression on Ficolled cord blood before and after AutoMACS enrichment. The CD34+ fraction obtained following AutoMACS was then sorted for the expression of CD34+CD38+ and CD34+CD38– cells. The CD34+CD38– cell population was then seeded onto OP9-control cells or OP9-DL1 cells. (B) CD34+CD38– cells sorted from human cord blood were cocultured with OP9-control (top 2 rows of histograms) or OP9-DL1 (bottom 2 rows of histograms) stromal cells for 49 days. Initiation of differentiation and maintenance of hematopoietic potential was evaluated approximately every 4 days of coculture through the loss and gain of CD34 and CD38 expression, respectively.
Figure 1.

Flow cytometric analysis of CD34 and CD38 expression following isolation from human cord blood and long-term coculture with OP9-control cells or OP9-DL1 cells. (A) Human HSCs were isolated into CD34+ and CD34 fractions from human cord blood following a CD34-positive selection protocol on AutoMACS. As a reference for fold enrichment, we show CD34 by CD38 expression on Ficolled cord blood before and after AutoMACS enrichment. The CD34+ fraction obtained following AutoMACS was then sorted for the expression of CD34+CD38+ and CD34+CD38 cells. The CD34+CD38 cell population was then seeded onto OP9-control cells or OP9-DL1 cells. (B) CD34+CD38 cells sorted from human cord blood were cocultured with OP9-control (top 2 rows of histograms) or OP9-DL1 (bottom 2 rows of histograms) stromal cells for 49 days. Initiation of differentiation and maintenance of hematopoietic potential was evaluated approximately every 4 days of coculture through the loss and gain of CD34 and CD38 expression, respectively.

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