The purpose of the publication was to investigate the molecular circadian clock in an Arctic context by contrasting reindeer with mouse fibroblast cell cultures. Cell cultures were transduced with promoter luciferase reporters for the clock genes Bmal1 and Per2. The data acquired from the promoter reporter measurements were to some extent confirmed by mRNA abundance measurements done by qPCR.
The data set published here contains the promoter reporter data, measured as bioluminescence in a PMT (photon multiplier tube) and qPCR data.
CircWave, Version 1.4
GraphPad Prism, Version 9.4.0
Photon Detection Unit - software, Lm2400v12
Rstudio, 2023.09.1 Build 494