Fig. 1.
Fig. 1. Purification of human CD41a+ cells. / An enriched population of MKs was isolated after labeling with anti–CD41a-FITC antibody and anti-FITC immunomagnetic microbeads in the presence of 2 inhibitors of MK activation, adenosine and theophylline. The cells were analyzed by flow cytometry after having been passed once (single pure) and twice (double pure) through a magnetic column. This technique resulted in the isolation of a 98% pure CD41a+ MK population.

Purification of human CD41a+ cells.

An enriched population of MKs was isolated after labeling with anti–CD41a-FITC antibody and anti-FITC immunomagnetic microbeads in the presence of 2 inhibitors of MK activation, adenosine and theophylline. The cells were analyzed by flow cytometry after having been passed once (single pure) and twice (double pure) through a magnetic column. This technique resulted in the isolation of a 98% pure CD41a+ MK population.

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