Fig. 14.
Fig. 14. PB Inc−CD34+ cells that express SDF-1 are in cycle. / Freshly isolated PB CD34+ cells were purified immediately after density gradient separation (Inc−). Cell cycle status of SDF-1–expressing cells was determined by using a dual staining for Ki67 expression and SDF-1 intracellular expression as indicated in “Materials and methods.” (A) The Ki67 expression allowed discrimination of G0 (Ki67−) from G1+S+G2/M (Ki67+) cells. Arbitrary quadrants were drawn on the basis of isotype-matched negative control. (B) The logarithm fluorescence of intracellular SDF-1 is expressed in channel numbers. Histograms show results from staining with SDF-1 mAb (solid histogram) and results from staining with irrelevant isotype-matched control antibody (open histogram). The histograms shown are for one experiment representative of the 3 performed.

PB IncCD34+ cells that express SDF-1 are in cycle.

Freshly isolated PB CD34+ cells were purified immediately after density gradient separation (Inc). Cell cycle status of SDF-1–expressing cells was determined by using a dual staining for Ki67 expression and SDF-1 intracellular expression as indicated in “Materials and methods.” (A) The Ki67 expression allowed discrimination of G0 (Ki67) from G1+S+G2/M (Ki67+) cells. Arbitrary quadrants were drawn on the basis of isotype-matched negative control. (B) The logarithm fluorescence of intracellular SDF-1 is expressed in channel numbers. Histograms show results from staining with SDF-1 mAb (solid histogram) and results from staining with irrelevant isotype-matched control antibody (open histogram). The histograms shown are for one experiment representative of the 3 performed.

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