Your privacy, your choice

We use essential cookies to make sure the site can function. We also use optional cookies for advertising, personalisation of content, usage analysis, and social media.

By accepting optional cookies, you consent to the processing of your personal data - including transfers to third parties. Some third parties are outside of the European Economic Area, with varying standards of data protection.

See our privacy policy for more information on the use of your personal data.

for further information and to change your choices.

Skip to main content
Fig. 3 | BMC Cancer

Fig. 3

From: Interactions between leukemia and feeders in co-cultivation under hypoxia

Fig. 3

Proliferation of NHDF and hMSCs cells under different cultivation conditions in the individual cultivation. Doubling time (A) of NHDF and hMSCs after 48 h of cultivation. Colony formation assay (CFU-F) (B) assesses colony formation efficiency and proliferative potential after 14 days under different cultivation conditions. Bar graphs show individual data points (dots) and SD. The numbers above the bars indicate the mean for each group. Light microscopy images (C) showing size and morphology of NHDF and hMSCs´ colonies (the scale bar in the images represents 200 μm). In (A) and (B), statistical analyses were performed using a nonparametric, two-tailed Mann–Whitney U test for two-sample comparisons. Statistical significance (p ≤ 0.05) is indicated in the graphs using symbols that denote significant differences between the following comparisons: * = all individual cultivation samples vs. NX αMEM individual control medium (for each cell type separately), # = HX individual cultivation samples vs. HX αMEM individual control medium, significance brackets = differences for cells cultivated in the same cultivation medium grown under NX vs. HX

Back to article page