<p>Huh7 cells were treated with various concentration of recombinant Human IL-32γ (0–0.4μg/ml, R&D Systems) for 48h followed by FITC–Annexin V/PI flow cytometry analyses. (A) A representative FITC–Annexin V/PI assay of Huh7 cells. (B) A statistical analyses of the percentage of annexin V-positive Huh7 cells. The results are presented as the mean ± SD of three independent experiments.</p
<p>Light microscope images (x100) of the cells taken on day 5 after treatment with 100 ng per ml of ...
<p>Ba/F3-mock growing with IL-3, Ba/F3-BCR-JAK2 and Ba/F3-TEL-JAK2 cells (10<sup>5</sup>/ml) were gr...
<p>Confluent HaCaT cell cultures were treated with 10 µg/ml of either the pathogenic anti-Dsg3 antib...
<p>Neutrophils were incubated with graded concentrations of IL-32γ or its vehicle. Cells were analyz...
<p>IL-32γ-delayed apoptosis is dependent on kinase activation. Neutrophils were pre-incubated 30 min...
<p>Neutrophils were incubated with IL-32γ (500 ng.ml-1) or its vehicle (CONT) for 48 hrs. Cells with...
<p>A, Apoptosis assay was performed after T24 cells were cultured in RPMI-1640 containing hWJMSC-MVs...
<p>. The fluorescence profile of untreated HeLa cells. Untreated HeLa cells were collected and incub...
<p>The expression of IL-32 in NK-92 cells was detected upon stimulation with an anti-NKP30 antibody ...
<p><b>A.</b> Flow cytometric analysis of PI-stained HCC cell lines, including HepG2, SMMC-7721, Bel-...
<p>HL-1 cells were pretreated as indicated. Then, (A) cells were treated with annexin-V/PI double st...
<p>Cells were treated with 10 µM etoposide to induce apoptosis. A) After 48 hours, cells were staine...
<p>The apoptosis rate was detected by flow cytometry using the Annexin V-fluorescein isothiocyanate/...
<p>HUVECs were stimulated with or without IL-1β at 10 ng/ml for 24 hours. Total RNA were isolated an...
<p>Untreated cells (A); cilengitide treated cells (B); RGDechi-hCit treated cells (C). Upper left qu...
<p>Light microscope images (x100) of the cells taken on day 5 after treatment with 100 ng per ml of ...
<p>Ba/F3-mock growing with IL-3, Ba/F3-BCR-JAK2 and Ba/F3-TEL-JAK2 cells (10<sup>5</sup>/ml) were gr...
<p>Confluent HaCaT cell cultures were treated with 10 µg/ml of either the pathogenic anti-Dsg3 antib...
<p>Neutrophils were incubated with graded concentrations of IL-32γ or its vehicle. Cells were analyz...
<p>IL-32γ-delayed apoptosis is dependent on kinase activation. Neutrophils were pre-incubated 30 min...
<p>Neutrophils were incubated with IL-32γ (500 ng.ml-1) or its vehicle (CONT) for 48 hrs. Cells with...
<p>A, Apoptosis assay was performed after T24 cells were cultured in RPMI-1640 containing hWJMSC-MVs...
<p>. The fluorescence profile of untreated HeLa cells. Untreated HeLa cells were collected and incub...
<p>The expression of IL-32 in NK-92 cells was detected upon stimulation with an anti-NKP30 antibody ...
<p><b>A.</b> Flow cytometric analysis of PI-stained HCC cell lines, including HepG2, SMMC-7721, Bel-...
<p>HL-1 cells were pretreated as indicated. Then, (A) cells were treated with annexin-V/PI double st...
<p>Cells were treated with 10 µM etoposide to induce apoptosis. A) After 48 hours, cells were staine...
<p>The apoptosis rate was detected by flow cytometry using the Annexin V-fluorescein isothiocyanate/...
<p>HUVECs were stimulated with or without IL-1β at 10 ng/ml for 24 hours. Total RNA were isolated an...
<p>Untreated cells (A); cilengitide treated cells (B); RGDechi-hCit treated cells (C). Upper left qu...
<p>Light microscope images (x100) of the cells taken on day 5 after treatment with 100 ng per ml of ...
<p>Ba/F3-mock growing with IL-3, Ba/F3-BCR-JAK2 and Ba/F3-TEL-JAK2 cells (10<sup>5</sup>/ml) were gr...
<p>Confluent HaCaT cell cultures were treated with 10 µg/ml of either the pathogenic anti-Dsg3 antib...