Figure 3.
Figure 3. Northern blot analysis of the 4 neutrophil cell populations after MACS purification. (A) Northern blot of total RNA from the 4 MACS-depleted cell populations. The blot was hybridized with probes against the granule proteins MPO, lactoferrin, and fMLP-R, which are expressed specifically in MBs/PMs, MCs/MMs, and BCs/SCs and PMNs, respectively. (B) Schematic representation of the hybridization intensities from panel A. For each probe, the cell population showing maximal expression is given the value 1; the expression levels in the other cell populations are shown relative to this. All expression levels are normalized to the 18S level. (C) Relative hybridization intensities of 18S and β-actin in the 4 cell populations. Data are based on 12 (18S) or 17 (β-actin) filters blotted with 5 μg RNA from each cell population. For each hybridization, the cell population with the strongest signal was given the value 1, and the other signal intensities were related to this.

Northern blot analysis of the 4 neutrophil cell populations after MACS purification. (A) Northern blot of total RNA from the 4 MACS-depleted cell populations. The blot was hybridized with probes against the granule proteins MPO, lactoferrin, and fMLP-R, which are expressed specifically in MBs/PMs, MCs/MMs, and BCs/SCs and PMNs, respectively. (B) Schematic representation of the hybridization intensities from panel A. For each probe, the cell population showing maximal expression is given the value 1; the expression levels in the other cell populations are shown relative to this. All expression levels are normalized to the 18S level. (C) Relative hybridization intensities of 18S and β-actin in the 4 cell populations. Data are based on 12 (18S) or 17 (β-actin) filters blotted with 5 μg RNA from each cell population. For each hybridization, the cell population with the strongest signal was given the value 1, and the other signal intensities were related to this.

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