Fig. 2.
Fig. 2. Flow cytometric analysis of CD34+, CD34+CD38+, and CD34+CD38− cell subsets used to initiate BMLTC. (A) Scatter diagram of CD34+ selected cells stained with FITC-labeled CD34 MoAb and PE-labeled CD38 MoAb, in which Log PE fluorescence intensity was displayed versus Log FITC fluorescence intensity. (B) CD34+ cells were gated and sorted. (C) A scatter diagram of gated CD34+ cells sorted for absence of the CD38 activation marker (most-primitive BM stem cells). (D) The log PE fluorescence intensity (CD38) of an affinity column purified CD34+ cell population was displayed versus Log PerCP-fluorescence intensity (CD4). Results of one representative experiment illustrated.

Flow cytometric analysis of CD34+, CD34+CD38+, and CD34+CD38 cell subsets used to initiate BMLTC. (A) Scatter diagram of CD34+ selected cells stained with FITC-labeled CD34 MoAb and PE-labeled CD38 MoAb, in which Log PE fluorescence intensity was displayed versus Log FITC fluorescence intensity. (B) CD34+ cells were gated and sorted. (C) A scatter diagram of gated CD34+ cells sorted for absence of the CD38 activation marker (most-primitive BM stem cells). (D) The log PE fluorescence intensity (CD38) of an affinity column purified CD34+ cell population was displayed versus Log PerCP-fluorescence intensity (CD4). Results of one representative experiment illustrated.

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