Total RNA was purified from HL-1 cardiomyocytes submitted to increasing durations (from 5 min to 24 hr of hypoxia) at 1% O
2, as well as from normoxic cardiomyocytes as a control. cDNA was synthesized and used for a Fluidigm deltagene PCR array dedicated to genes related to (lymph)angiogenesis or stress (
Supplementary file 6). Relative quantification (RQ) of gene expression during hypoxia was calculated using the 2
–ΔΔCT method with normalization to 18S and to normoxia. The percentages of repressed (red), induced (green) and non-regulated (blue) mRNAs are shown for the shorter durations of hypoxia. The data for the longer durations are shown in
Figure 1. The threshold was set at 1.5 as in
Figure 1. The detailed values for all of the durations of hypoxia are presented in
Supplementary file 1.