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The housekeeping gene 18S was used to normalize levels of cDNA expression for each sample.
An atlas of the nasal mucosa is automatically detected and used to normalize levels of enhancement.
The relative abundance of βactin mRNA was used to normalize levels of- MMP-1 mRNAs.
The relative abundance of GAPDH mRNA was used to normalize levels of the mRNAs of interest.
β -Actin mRNA was used to normalize levels of the mRNAs of interest.
The I. scapularis β-Actin, Cyclophilin A genes were used to normalize levels of mRNA in all samples (Table 1).
Similar(51)
RPLP0 mRNA levels were used to normalize the levels of genes of interests.
The 2-ΔΔCt method was used to normalize transcription levels to human 18S or Mus β-actin and to calculate fold-changes in expression levels relative to controls.
The level of LDH release following exposure to S. coelicolor conditioned media was used to normalize the levels of LDH release observed following S. venezuelae treatment to standardize the values.
β-actin expression was used to normalize transcript levels.
Reference genes, often also referred to as calibrator genes are used to normalize RNA levels between different samples.
More suggestions(15)
used to characterize levels
used to normalize transfections
used to define levels
used to derive levels
used to detect levels
used to adjust levels
used to quantitate levels
used to control levels
used to gain levels
used to measure levels
used to decrease levels
used to quantify levels
used to normalize values
used to normalize samples
used to raise levels
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