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Exact(8)
Results were normalized using the reference genes cyclophilin or ubiquitin, which showed minimal changes in their level of expression in the array data.
All transcript values were normalized using the reference genes ARF2, PTB, SAND, and ORE9 identified by Chao et al. [ 97].
Therefore, normalization of the data was done using the reference genes Hypoxanthine (Hipox) and Peptidylprolyl Isomerase A (Ppia).
The results were used to calculate relative quantity of expression of the different genes, using the reference genes GAPDH and HPRT1 for normalisation.
For each gene, the mean value only of the assays with a comparable trend was calculated and normalized using the reference genes.
Ct values for the target genes were normalized using the reference genes hisC, rpoA and sigA, which showed no variation in the corresponding transcript levels for the experimental conditions used (data not shown).
Similar(52)
The data were normalized using the reference gene, β-actin, and are corrected for PCR efficiencies.
The obtained data were standardized using the reference gene, β-actin.
For the data presented here, δ k can be estimated using the reference gene, Becn1.
GLP1R expression analysis was quantified using the reference gene β-actin.
A 10-fold dilution series was conducted on one patient's cDNA using the reference gene TBP to test for inhibitory components in the tissue.
More suggestions(15)
using the target genes
using the reference signals
using the reference frames
using the seed genes
using the amoCAB genes
using the reference channels
using the candidate genes
using the nonzero genes
using the reference values
using the reference correlations
using the reference samples
using the reporter genes
using the reference data
using the intersection genes
using the housekeeping genes
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