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Empty wells were used as negative control.
DMEM culture medium was used as negative control.
Non-pulsed targets were used as negative controls.
ACT2 was used as negative control for H3K27me3 distribution.
Non-transfected EPSCs (DR25) were used as negative control.
Cells without drug incubation were used as negative control.
Sterile water was used as negative control for DNA amplification, and DNAse treated RNA before reverse transcription was used as negative control for cDNA amplification.
Untreated substrate was used as negative control.
Distilled water was used as negative control.
ddH2O was used as negative control (N.C).
Escherichia coli was used as negative control.
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