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Each level was analyzed to check for its signal-to-noise (S/N) ratio and the associated UV spectrum.
Mutants with t-DNA insertion in the candidate genes can also be searched in OrygenesDB, their expression in root tissues checked by using Oryza-Tag Line GFP andataP data (Larmande et al. 2008) and the mutants analyzed to check for the mutation effect on root morphology or development.
The samples were then centrifuged at 400 g and the serum was filtered through a 0.22 μm filter into sterile plastic culture tubes. 100 μL of 99mTc labeled formulations were incubated respectively in 900 μL of this serum (in duplicate) at 37°C and analyzed to check for any dissociation of the complex by ITLC using silica gel strips and 0.9% NaCl aqueous solution (saline) as developing solvent.
Samples of the fixative were analyzed to check for Hg content.
A short 125 bp fragment of STOX1 (locus 10q21.3) was analyzed to check for potential PCR inhibition.
Resulting colonies (n = 288) were isolated and analyzed to check for positive clones and to choose clones with different restriction profiles.
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Results of bacterial diversity obtained for bioreactors Lab MBR and Low Temperature CANON were further analyzed to check the performance of primer 530F for the evaluation of anammox diversity.
Melting curves for each sample were analyzed to check the specificity of amplification.
Conventional samples were also analyzed in order to check for PCR and/or seed contaminants.
Poly(A -tails represent the only generA -tails that can be analyzed using SAGE to check forepresentl mRNA degradathen.
Each MEKK1 mutant was overexpressed in 293T cells in the highly expressing pApuro vector and analyzed via western blot to check for protein expression.
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